Allele Registry

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.5986976T>G , CM000669.2:g.5986976T>G	GRCh38
NC_000007.13:g.6026607T>G , CM000669.1:g.6026607T>G	GRCh37
NC_000007.12:g.5993133T>G	NCBI36
NG_008466.1:g.27131A>C , LRG_161:g.27131A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000699814.2:c.*1185A>C	ENSP00000514615.2:n.*1185A>C
ENST00000699840.2:c.1786A>C	ENSP00000514638.2:p.Thr596Pro
ENST00000699930.2:c.1681A>C	ENSP00000514695.2:p.Thr561Pro
ENST00000406569.8:c.1678+111A>C	ENSP00000514464.1:n.1678+111A>C
ENST00000644110.2:c.*1383A>C	ENSP00000496392.2:n.*1383A>C
ENST00000699752.1:c.1633A>C	ENSP00000514561.1:p.Thr545Pro
ENST00000699753.1:c.*1210A>C	ENSP00000514562.1:n.*1210A>C
ENST00000699754.1:c.1591A>C	ENSP00000514563.1:p.Thr531Pro
ENST00000699755.1:c.*1188A>C	ENSP00000514564.1:n.*1188A>C
ENST00000699756.1:c.*1376A>C	ENSP00000514565.1:n.*1376A>C
ENST00000699757.1:c.*1046A>C	ENSP00000514566.1:n.*1046A>C
ENST00000699758.1:c.*1046A>C	ENSP00000514567.1:n.*1046A>C
ENST00000699759.1:n.2643A>C
ENST00000699760.1:c.1471A>C	ENSP00000514568.1:p.Thr491Pro
ENST00000699761.1:c.1384A>C	ENSP00000514569.1:p.Thr462Pro
ENST00000699762.1:c.1216A>C	ENSP00000514570.1:p.Thr406Pro
ENST00000699763.1:c.*879A>C	ENSP00000514571.1:n.*879A>C
ENST00000699764.1:c.*107A>C	ENSP00000514572.1:n.*107A>C
ENST00000699765.1:c.*885A>C	ENSP00000514573.1:n.*885A>C
ENST00000699766.1:c.1789A>C	ENSP00000514574.1:p.Thr597Pro
ENST00000699767.1:c.1789A>C	ENSP00000514575.1:p.Thr597Pro
ENST00000699768.1:c.1789A>C	ENSP00000514576.1:p.Thr597Pro
ENST00000699811.1:c.1384A>C	ENSP00000514614.1:p.Thr462Pro
ENST00000699813.1:n.1902A>C
ENST00000699814.1:c.1412A>C
ENST00000699815.1:c.*1320A>C	ENSP00000514616.1:n.*1320A>C
ENST00000699816.1:c.*679A>C	ENSP00000514617.1:n.*679A>C
ENST00000699817.1:c.*1383A>C	ENSP00000514618.1:n.*1383A>C
ENST00000699818.1:c.1384A>C	ENSP00000514619.1:p.Thr462Pro
ENST00000699819.1:c.*946A>C	ENSP00000514620.1:n.*946A>C
ENST00000699820.1:c.1144+2824A>C	ENSP00000514621.1:n.1144+2824A>C
ENST00000699821.1:c.1384A>C	ENSP00000514622.1:p.Thr462Pro
ENST00000699822.1:c.*1241A>C	ENSP00000514623.1:n.*1241A>C
ENST00000699823.1:c.1384A>C	ENSP00000514624.1:p.Thr462Pro
ENST00000699824.1:c.*1292A>C	ENSP00000514625.1:n.*1292A>C
ENST00000699825.1:c.1228A>C	ENSP00000514626.1:p.Thr410Pro
ENST00000699826.1:c.*1188A>C	ENSP00000514627.1:n.*1188A>C
ENST00000699827.1:c.1621A>C	ENSP00000514628.1:p.Thr541Pro
ENST00000699828.1:c.*879A>C	ENSP00000514629.1:n.*879A>C
ENST00000699833.1:n.3561A>C
ENST00000699837.1:c.1384A>C	ENSP00000514635.1:p.Thr462Pro
ENST00000699838.1:c.*1689A>C	ENSP00000514636.1:n.*1689A>C
ENST00000699839.1:c.1975A>C	ENSP00000514637.1:p.Thr659Pro
ENST00000699916.1:c.*1046A>C	ENSP00000514684.1:n.*1046A>C
ENST00000699917.1:c.*1238A>C	ENSP00000514685.1:n.*1238A>C
ENST00000699918.1:c.*1290A>C	ENSP00000514686.1:n.*1290A>C
ENST00000699919.1:c.*1376A>C	ENSP00000514687.1:n.*1376A>C
ENST00000699920.1:c.*1425A>C	ENSP00000514688.1:n.*1425A>C
ENST00000699928.1:c.989-3985A>C	ENSP00000514693.1:n.989-3985A>C
ENST00000699929.1:c.*1090A>C	ENSP00000514694.1:n.*1090A>C
ENST00000699930.1:c.1681A>C	ENSP00000514695.1:p.Thr561Pro
ENST00000699931.1:n.3217A>C
ENST00000699951.1:c.*885A>C	ENSP00000514706.1:n.*885A>C
ENST00000699952.1:c.803+10350A>C	ENSP00000514707.1:n.803+10350A>C
ENST00000699953.1:c.*896A>C	ENSP00000514708.1:n.*896A>C
ENST00000699954.1:c.*1090A>C	ENSP00000514709.1:n.*1090A>C
ENST00000265849.12:c.1789A>C MANE Select	ENSP00000265849.7:p.Thr597Pro
ENST00000642292.1:c.1384A>C	ENSP00000495524.1:p.Thr462Pro
ENST00000642456.1:c.1384A>C	ENSP00000493814.1:p.Thr462Pro
ENST00000643595.1:c.*1188A>C	ENSP00000494497.1:n.*1188A>C
ENST00000644110.1:c.1471A>C	ENSP00000496392.1:p.Thr491Pro
ENST00000265849.11:c.1789A>C	ENSP00000265849.7:p.Thr597Pro
ENST00000382321.5:c.804-3985A>C	ENSP00000371758.4:n.804-3985A>C
ENST00000406569.7:n.1678+111A>C
ENST00000441476.6:c.1471A>C	ENSP00000392843.2:p.Thr491Pro
ENST00000469652.1:n.63-4071A>C
NM_000535.5:c.1789A>C , LRG_161t1:c.1789A>C	NP_000526.1:p.Thr597Pro
NR_003085.2:n.1871A>C
XM_006715742.2:c.1783A>C	XP_006715805.1:p.Thr595Pro
XM_006715744.2:c.856A>C	XP_006715807.1:p.Thr286Pro
XM_011515427.1:c.1834A>C	XP_011513729.1:p.Thr612Pro
XM_011515428.1:c.1678A>C	XP_011513730.1:p.Thr560Pro
XM_011515429.1:c.1471A>C	XP_011513731.1:p.Thr491Pro
XM_011515430.1:c.1471A>C	XP_011513732.1:p.Thr491Pro
NM_000535.6:c.1789A>C	NP_000526.2:p.Thr597Pro
NM_001322003.1:c.1384A>C	NP_001308932.1:p.Thr462Pro
NM_001322004.1:c.1384A>C	NP_001308933.1:p.Thr462Pro
NM_001322005.1:c.1384A>C	NP_001308934.1:p.Thr462Pro
NM_001322006.1:c.1633A>C	NP_001308935.1:p.Thr545Pro
NM_001322007.1:c.1471A>C	NP_001308936.1:p.Thr491Pro
NM_001322008.1:c.1471A>C	NP_001308937.1:p.Thr491Pro
NM_001322009.1:c.1384A>C	NP_001308938.1:p.Thr462Pro
NM_001322010.1:c.1228A>C	NP_001308939.1:p.Thr410Pro
NM_001322011.1:c.856A>C	NP_001308940.1:p.Thr286Pro
NM_001322012.1:c.856A>C	NP_001308941.1:p.Thr286Pro
NM_001322013.1:c.1216A>C	NP_001308942.1:p.Thr406Pro
NM_001322014.1:c.1789A>C	NP_001308943.1:p.Thr597Pro
NM_001322015.1:c.1480A>C	NP_001308944.1:p.Thr494Pro
NR_136154.1:n.1876A>C
XM_006715744.4:c.856A>C	XP_006715807.1:p.Thr286Pro
XM_017012342.2:c.856A>C	XP_016867831.1:p.Thr286Pro
XM_024446800.1:c.1228A>C	XP_024302568.1:p.Thr410Pro
NM_000535.7:c.1789A>C MANE Select	NP_000526.2:p.Thr597Pro
NM_001322003.2:c.1384A>C	NP_001308932.1:p.Thr462Pro
NM_001322004.2:c.1384A>C	NP_001308933.1:p.Thr462Pro
NM_001322005.2:c.1384A>C	NP_001308934.1:p.Thr462Pro
NM_001322006.2:c.1633A>C	NP_001308935.1:p.Thr545Pro
NM_001322008.2:c.1471A>C	NP_001308937.1:p.Thr491Pro
NM_001322009.2:c.1384A>C	NP_001308938.1:p.Thr462Pro
NM_001322010.2:c.1228A>C	NP_001308939.1:p.Thr410Pro
NM_001322011.2:c.856A>C	NP_001308940.1:p.Thr286Pro
NM_001322012.2:c.856A>C	NP_001308941.1:p.Thr286Pro
NM_001322013.2:c.1216A>C	NP_001308942.1:p.Thr406Pro
NM_001322014.2:c.1789A>C	NP_001308943.1:p.Thr597Pro
NM_001322015.2:c.1480A>C	NP_001308944.1:p.Thr494Pro
NM_001322007.2:c.1471A>C	NP_001308936.1:p.Thr491Pro

Linked Data

Genomic Alleles

Transcript Alleles