Canonical Allele Identifier: CA368228223

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.94588691G>A , CM000669.2:g.94588691G>A GRCh38
NC_000007.13:g.94218003G>A , CM000669.1:g.94218003G>A GRCh37
NC_000007.12:g.94055939G>A NCBI36
NG_008893.1:g.72519C>T
NG_008893.2:g.72519C>T
NG_008893.3:g.72882C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000415788.3:c.1403C>T (SGCE) ENSP00000405313.2:p.Thr468Ile
ENST00000428696.7:c.1247C>T (SGCE) ENSP00000397536.3:p.Thr416Ile
ENST00000437425.7:c.1172C>T (SGCE) ENSP00000394061.2:p.Thr391Ile
ENST00000445866.7:c.1370C>T (SGCE) ENSP00000398930.2:p.Thr457Ile
ENST00000447873.6:c.1268C>T (SGCE) ENSP00000388734.1:p.Thr423Ile
ENST00000642291.1:c.1230C>T (SGCE)
ENST00000642353.1:n.1522C>T (SGCE)
ENST00000642394.1:c.1145C>T (SGCE) ENSP00000493751.1:p.Thr382Ile
ENST00000642441.1:c.1349C>T (SGCE) ENSP00000495994.1:p.Thr450Ile
ENST00000642497.1:n.2041C>T (SGCE)
ENST00000642638.1:c.*1333C>T (SGCE) ENSP00000495555.1:n.*1333C>T
ENST00000642707.1:c.1451C>T (SGCE) ENSP00000495270.1:p.Thr484Ile
ENST00000642754.1:n.6126-3176C>T (SGCE)
ENST00000642759.1:n.1613C>T (SGCE)
ENST00000642802.1:n.1090C>T (SGCE)
ENST00000642904.1:n.1612C>T (SGCE)
ENST00000642933.1:c.1268C>T (SGCE) ENSP00000496237.1:p.Thr423Ile
ENST00000643041.1:c.*256C>T (SGCE) ENSP00000495311.1:n.*256C>T
ENST00000643160.1:c.526C>T (SGCE)
ENST00000643193.1:c.1268C>T (SGCE) ENSP00000496559.1:p.Thr423Ile
ENST00000643206.1:c.*876C>T (SGCE) ENSP00000496172.1:n.*876C>T
ENST00000643272.1:c.1376C>T (SGCE) ENSP00000494488.1:p.Thr459Ile
ENST00000643324.1:n.2186C>T (SGCE)
ENST00000643491.1:n.1196C>T (SGCE)
ENST00000643568.1:c.1064C>T (SGCE)
ENST00000643605.1:c.*1255C>T (SGCE) ENSP00000496480.1:n.*1255C>T
ENST00000643610.1:c.*96C>T (SGCE) ENSP00000494350.1:n.*96C>T
ENST00000643714.1:n.1336C>T (SGCE)
ENST00000643991.1:c.1177C>T (SGCE)
ENST00000644087.1:c.*1345C>T (SGCE) ENSP00000495249.1:n.*1345C>T
ENST00000644116.1:c.1343C>T (SGCE) ENSP00000495276.1:p.Thr448Ile
ENST00000644122.1:c.1376C>T (SGCE) ENSP00000495236.1:p.Thr459Ile
ENST00000644268.1:n.1888C>T (SGCE)
ENST00000644373.1:n.2304C>T (SGCE)
ENST00000644375.1:c.1334C>T (SGCE) ENSP00000494315.1:p.Thr445Ile
ENST00000644533.1:n.2050C>T (SGCE)
ENST00000644551.1:c.1376C>T (SGCE) ENSP00000493981.1:p.Thr459Ile
ENST00000644609.1:c.1268C>T (SGCE) ENSP00000496045.1:p.Thr423Ile
ENST00000644639.1:c.*929C>T (SGCE) ENSP00000496391.1:n.*929C>T
ENST00000644658.1:c.647C>T (SGCE)
ENST00000644674.1:n.1196C>T (SGCE)
ENST00000644681.1:c.995C>T (SGCE) ENSP00000496455.1:p.Thr332Ile
ENST00000644682.1:c.1332C>T (SGCE)
ENST00000644816.1:c.1295C>T (SGCE) ENSP00000494898.1:p.Thr432Ile
ENST00000645101.1:c.1457C>T (SGCE) ENSP00000494975.1:p.Thr486Ile
ENST00000645262.1:c.1145C>T (SGCE) ENSP00000494164.1:p.Thr382Ile
ENST00000645445.1:c.1242C>T (SGCE)
ENST00000645535.1:c.995C>T (SGCE) ENSP00000493984.1:p.Thr332Ile
ENST00000645579.1:n.2188C>T (SGCE)
ENST00000645624.1:n.831C>T (SGCE)
ENST00000645665.1:n.514C>T (SGCE)
ENST00000645725.1:c.1349C>T (SGCE) ENSP00000495480.1:p.Thr450Ile
ENST00000645767.1:n.1331C>T (SGCE)
ENST00000645804.1:c.98C>T (SGCE) ENSP00000494688.1:p.Thr33Ile
ENST00000646098.1:c.1271C>T (SGCE) ENSP00000495591.1:p.Thr424Ile
ENST00000646119.1:c.1269C>T (SGCE)
ENST00000646137.1:c.1268C>T (SGCE) ENSP00000495199.1:p.Thr423Ile
ENST00000646265.1:c.1357C>T (SGCE)
ENST00000646301.1:c.1241C>T (SGCE)
ENST00000646434.1:c.1517C>T (SGCE)
ENST00000646466.1:c.*1273C>T (SGCE) ENSP00000493511.1:n.*1273C>T
ENST00000646489.1:c.1403C>T (SGCE) ENSP00000496268.1:p.Thr468Ile
ENST00000646559.1:c.*1225C>T (SGCE) ENSP00000495838.1:n.*1225C>T
ENST00000646600.1:c.*1198C>T (SGCE) ENSP00000494041.1:n.*1198C>T
ENST00000646879.1:c.1268C>T (SGCE) ENSP00000495209.1:p.Thr423Ile
ENST00000646910.1:n.1328C>T (SGCE)
ENST00000646943.1:c.1370C>T (SGCE) ENSP00000494666.1:p.Thr457Ile
ENST00000647018.1:c.1362-3176C>T (SGCE) ENSP00000493722.1:n.1362-3176C>T
ENST00000647031.1:n.3841-3176C>T (SGCE)
ENST00000647048.1:c.1092C>T (SGCE)
ENST00000647096.1:c.1484C>T (SGCE) ENSP00000494192.1:p.Thr495Ile
ENST00000647110.1:c.1274C>T (SGCE) ENSP00000494738.1:p.Thr425Ile
ENST00000647334.1:c.1374C>T (SGCE)
ENST00000647351.1:c.1376C>T (SGCE) ENSP00000494556.1:p.Thr459Ile
ENST00000647533.1:n.2916C>T (SGCE)
ENST00000648936.2:c.1295C>T (SGCE) MANE Select ENSP00000497130.1:p.Thr432Ile
ENST00000265735.11:c.1295C>T (SGCE) ENSP00000265735.6:p.Thr432Ile
ENST00000415788.2:c.1403C>T (SGCE) ENSP00000405313.2:p.Thr468Ile
ENST00000428696.6:c.1268C>T (SGCE) ENSP00000397536.2:p.Thr423Ile
ENST00000437425.6:c.1172C>T (SGCE) ENSP00000394061.2:p.Thr391Ile
ENST00000445866.6:c.1370C>T (SGCE) ENSP00000398930.2:p.Thr457Ile
ENST00000447873.5:c.1268C>T (SGCE) ENSP00000388734.1:p.Thr423Ile
ENST00000472326.2:n.405C>T (SGCE)
ENST00000522045.5:c.123-3176C>T (SGCE) ENSP00000431080.1:n.123-3176C>T
NM_001099400.1:c.1268C>T (SGCE) NP_001092870.1:p.Thr423Ile
NM_001099401.1:c.1370C>T (SGCE) NP_001092871.1:p.Thr457Ile
NM_001301139.1:c.1172C>T (SGCE) NP_001288068.1:p.Thr391Ile
NM_003919.2:c.1295C>T (SGCE) NP_003910.1:p.Thr432Ile
XM_005250675.3:c.1403C>T (SGCE) XP_005250732.1:p.Thr468Ile
XM_005250677.3:c.1376C>T (SGCE) XP_005250734.1:p.Thr459Ile
XM_011516495.1:c.2127+34116G>A (CASD1) XP_011514797.1:n.2127+34116G>A
XM_011516663.1:c.1403C>T (SGCE) XP_011514965.1:p.Thr468Ile
XM_011516664.1:c.1376C>T (SGCE) XP_011514966.1:p.Thr459Ile
XM_011516665.1:c.1295C>T (SGCE) XP_011514967.1:p.Thr432Ile
XM_011516666.1:c.1268C>T (SGCE) XP_011514968.1:p.Thr423Ile
XM_011516667.1:c.1208C>T (SGCE) XP_011514969.1:p.Thr403Ile
XM_011516668.1:c.1172C>T (SGCE) XP_011514970.1:p.Thr391Ile
XM_011516669.1:c.1022C>T (SGCE) XP_011514971.1:p.Thr341Ile
NM_001346713.1:c.1403C>T (SGCE) NP_001333642.1:p.Thr468Ile
NM_001346715.1:c.1376C>T (SGCE) NP_001333644.1:p.Thr459Ile
NM_001346717.1:c.1268C>T (SGCE) NP_001333646.1:p.Thr423Ile
NM_001346719.1:c.1208C>T (SGCE) NP_001333648.1:p.Thr403Ile
NM_001346720.1:c.1022C>T (SGCE) NP_001333649.1:p.Thr341Ile
NM_001362807.1:c.1181C>T (SGCE) NP_001349736.1:p.Thr394Ile
NM_001362808.1:c.995C>T (SGCE) NP_001349737.1:p.Thr332Ile
NM_001362809.1:c.1145C>T (SGCE) NP_001349738.1:p.Thr382Ile
XM_011516495.2:c.2127+34116G>A (CASD1) XP_011514797.1:n.2127+34116G>A
XM_011516663.2:c.1403C>T (SGCE) XP_011514965.1:p.Thr468Ile
XM_011516664.2:c.1376C>T (SGCE) XP_011514966.1:p.Thr459Ile
XM_011516665.3:c.1295C>T (SGCE) XP_011514967.1:p.Thr432Ile
XM_011516666.3:c.1268C>T (SGCE) XP_011514968.1:p.Thr423Ile
XM_011516667.2:c.1208C>T (SGCE) XP_011514969.1:p.Thr403Ile
XM_011516669.3:c.1022C>T (SGCE) XP_011514971.1:p.Thr341Ile
XM_017012763.1:c.1208C>T (SGCE) XP_016868252.1:p.Thr403Ile
XM_017012767.1:c.995C>T (SGCE) XP_016868256.1:p.Thr332Ile
XM_024446985.1:c.1172C>T (SGCE) XP_024302753.1:p.Thr391Ile
XM_024446986.1:c.1145C>T (SGCE) XP_024302754.1:p.Thr382Ile
NM_001099400.2:c.1268C>T (SGCE) NP_001092870.1:p.Thr423Ile
NM_001099401.2:c.1370C>T (SGCE) NP_001092871.1:p.Thr457Ile
NM_001301139.2:c.1172C>T (SGCE) NP_001288068.1:p.Thr391Ile
NM_001346713.2:c.1403C>T (SGCE) NP_001333642.1:p.Thr468Ile
NM_001346715.2:c.1376C>T (SGCE) NP_001333644.1:p.Thr459Ile
NM_001346717.2:c.1268C>T (SGCE) NP_001333646.1:p.Thr423Ile
NM_001346719.2:c.1208C>T (SGCE) NP_001333648.1:p.Thr403Ile
NM_001346720.2:c.1022C>T (SGCE) NP_001333649.1:p.Thr341Ile
NM_001362807.2:c.1181C>T (SGCE) NP_001349736.1:p.Thr394Ile
NM_001362808.2:c.995C>T (SGCE) NP_001349737.1:p.Thr332Ile
NM_001362809.2:c.1145C>T (SGCE) NP_001349738.1:p.Thr382Ile
NM_003919.3:c.1295C>T (SGCE) MANE Select NP_003910.1:p.Thr432Ile