Canonical Allele Identifier: CA1881752614
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518888G= , CM000671.2:g.131518888G= GRCh38
NC_000009.11:g.134394275G= , CM000671.1:g.134394275G= GRCh37
NC_000009.10:g.133384096G= NCBI36
NG_008896.1:g.20987G=
NG_008896.2:g.20987G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1255G= ENSP00000343034.7:p.Gly419=
ENST00000404875.7:n.1957G=
ENST00000423007.6:c.1474G= ENSP00000404119.2:p.Gly492=
ENST00000677295.2:c.*1761G= ENSP00000504346.2:n.*1761G=
ENST00000678264.2:c.*1600G= ENSP00000503157.2:n.*1600G=
ENST00000682070.1:n.1882G=
ENST00000682539.1:c.355G=
ENST00000682813.1:n.1821G=
ENST00000683392.1:n.4164G=
ENST00000683712.1:n.1822G=
ENST00000683900.1:n.3317G=
ENST00000684062.1:n.2083G=
ENST00000684579.1:n.3263G=
ENST00000684679.1:n.644G=
ENST00000341012.12:c.1255G= ENSP00000343034.7:p.Gly419=
ENST00000372220.5:c.286G= ENSP00000361294.5:p.Gly96=
ENST00000372228.9:c.1483G= ENSP00000361302.3:p.Gly495=
ENST00000402686.8:c.1417G= MANE Select ENSP00000385797.4:p.Gly473=
ENST00000676640.1:c.1417G= ENSP00000503281.1:p.Gly473=
ENST00000676803.1:c.592G= ENSP00000503093.1:p.Gly198=
ENST00000676835.1:c.*632G= ENSP00000502911.1:n.*632G=
ENST00000677029.1:c.961G= ENSP00000502936.1:p.Gly321=
ENST00000677099.1:c.*1127G= ENSP00000504553.1:n.*1127G=
ENST00000677216.1:c.1066G= ENSP00000503772.1:p.Gly356=
ENST00000677221.1:n.442G=
ENST00000677295.1:c.*794G= ENSP00000504346.1:n.*794G=
ENST00000677444.1:c.1362G=
ENST00000677586.1:n.898G=
ENST00000677626.1:c.1066G= ENSP00000503552.1:p.Gly356=
ENST00000677677.1:n.1377G=
ENST00000677853.1:c.*425G= ENSP00000503488.1:n.*425G=
ENST00000678202.1:n.576G=
ENST00000678264.1:c.*794G= ENSP00000503157.1:n.*794G=
ENST00000678303.1:c.1327G= ENSP00000503696.1:p.Gly443=
ENST00000678366.1:c.*1666G= ENSP00000504353.1:n.*1666G=
ENST00000678546.1:c.*1362G= ENSP00000503062.1:n.*1362G=
ENST00000678548.1:c.*1489G= ENSP00000503934.1:n.*1489G=
ENST00000678626.1:n.1253G=
ENST00000678733.1:c.498G=
ENST00000678739.1:c.*1743G= ENSP00000503806.1:n.*1743G=
ENST00000678833.1:c.*864G= ENSP00000503893.1:n.*864G=
ENST00000679023.1:c.1255G= ENSP00000503718.1:p.Gly419=
ENST00000679076.1:c.1036G=
ENST00000679111.1:c.*173G= ENSP00000504257.1:n.*173G=
ENST00000679189.1:c.1066G= ENSP00000503356.1:p.Gly356=
ENST00000341012.11:c.1255G= ENSP00000343034.7:p.Gly419=
ENST00000372220.4:c.280G= ENSP00000361294.4:p.Gly94=
ENST00000372228.7:c.1483G= ENSP00000361302.3:p.Gly495=
ENST00000402686.7:c.1417G= ENSP00000385797.3:p.Gly473=
ENST00000404875.6:c.1066G= ENSP00000384531.2:p.Gly356=
ENST00000423007.5:c.1417G= ENSP00000404119.1:p.Gly473=
ENST00000467848.1:n.121G=
ENST00000485278.5:n.1972G=
NM_001077365.1:c.1417G= NP_001070833.1:p.Gly473=
NM_001077366.1:c.1255G= NP_001070834.1:p.Gly419=
NM_001136113.1:c.1417G= NP_001129585.1:p.Gly473=
NM_001136114.1:c.1066G= NP_001129586.1:p.Gly356=
NM_007171.3:c.1483G= NP_009102.3:p.Gly495=
XM_005272156.1:c.1483G= XP_005272213.1:p.Gly495=
XM_005272158.1:c.1321G= XP_005272215.1:p.Gly441=
XM_005272159.1:c.1132G= XP_005272216.1:p.Gly378=
XM_005272162.1:c.286G= XP_005272219.1:p.Gly96=
XM_006716932.1:c.1132G= XP_006716995.1:p.Gly378=
XM_011518140.1:c.1336G= XP_011516442.1:p.Gly446=
XM_011518141.1:c.1270G= XP_011516443.1:p.Gly424=
XM_011518142.1:c.1174G= XP_011516444.1:p.Gly392=
XM_011518143.1:c.1168G= XP_011516445.1:p.Gly390=
XM_011518144.1:c.*173G= XP_011516446.1:n.*173G=
XM_011518145.1:c.1027G= XP_011516447.1:p.Gly343=
XM_011518146.1:c.*173G= XP_011516448.1:n.*173G=
XM_011518147.1:c.355G= XP_011516449.1:p.Gly119=
XR_929703.1:n.1659G=
NM_001353193.1:c.1483G= NP_001340122.1:p.Gly495=
NM_001353194.1:c.1255G= NP_001340123.1:p.Gly419=
NM_001353195.1:c.1066G= NP_001340124.1:p.Gly356=
NM_001353196.1:c.1327G= NP_001340125.1:p.Gly443=
NM_001353197.1:c.1321G= NP_001340126.1:p.Gly441=
NM_001353198.1:c.1321G= NP_001340127.1:p.Gly441=
NM_001353199.1:c.1132G= NP_001340128.1:p.Gly378=
NM_001353200.1:c.961G= NP_001340129.1:p.Gly321=
NR_148391.1:n.1467G=
NR_148392.1:n.1685G=
NR_148393.1:n.1606G=
NR_148394.1:n.1360G=
NR_148395.1:n.1758G=
NR_148396.1:n.1392G=
NR_148397.1:n.1517G=
NR_148398.1:n.1472G=
NR_148399.1:n.1998G=
NR_148400.1:n.1597G=
XM_005272162.3:c.286G= XP_005272219.1:p.Gly96=
XM_006716932.2:c.1132G= XP_006716995.1:p.Gly378=
XM_011518140.2:c.1336G= XP_011516442.1:p.Gly446=
XM_011518141.2:c.1270G= XP_011516443.1:p.Gly424=
XM_011518142.2:c.1174G= XP_011516444.1:p.Gly392=
XM_011518143.2:c.1168G= XP_011516445.1:p.Gly390=
XM_011518145.2:c.1027G= XP_011516447.1:p.Gly343=
XM_017014205.2:c.286G= XP_016869694.1:p.Gly96=
XM_024447380.1:c.286G= XP_024303148.1:p.Gly96=
XM_024447381.1:c.592G= XP_024303149.1:p.Gly198=
XM_024447382.1:c.286G= XP_024303150.1:p.Gly96=
XR_001746160.2:n.1587G=
XR_001746162.2:n.1792G=
XR_001746164.1:n.1509G=
XR_001746166.2:n.1804G=
NM_001077365.2:c.1417G= MANE Select NP_001070833.1:p.Gly473=
NM_001077366.2:c.1255G= NP_001070834.1:p.Gly419=
NM_001136113.2:c.1417G= NP_001129585.1:p.Gly473=
NM_001136114.2:c.1066G= NP_001129586.1:p.Gly356=
NM_001353193.2:c.1483G= NP_001340122.2:p.Gly495=
NM_001353194.2:c.1255G= NP_001340123.1:p.Gly419=
NM_001353195.2:c.1066G= NP_001340124.1:p.Gly356=
NM_001353196.2:c.1327G= NP_001340125.1:p.Gly443=
NM_001353197.2:c.1321G= NP_001340126.2:p.Gly441=
NM_001353198.2:c.1321G= NP_001340127.2:p.Gly441=
NM_001353199.2:c.1132G= NP_001340128.2:p.Gly378=
NM_001353200.2:c.961G= NP_001340129.1:p.Gly321=
NM_001374689.1:c.1405G= NP_001361618.1:p.Gly469=
NM_001374690.1:c.1365+351G= NP_001361619.1:n.1365+351G=
NM_001374691.1:c.1066G= NP_001361620.1:p.Gly356=
NM_001374692.1:c.1066G= NP_001361621.1:p.Gly356=
NM_001374693.1:c.1066G= NP_001361622.1:p.Gly356=
NM_001374695.1:c.1027G= NP_001361624.1:p.Gly343=
NM_007171.4:c.1483G= NP_009102.4:p.Gly495=
NR_148391.2:n.1451G=
NR_148392.2:n.1669G=
NR_148393.2:n.1590G=
NR_148394.2:n.1344G=
NR_148395.2:n.1742G=
NR_148396.2:n.1376G=
NR_148397.2:n.1501G=
NR_148398.2:n.1456G=
NR_148399.2:n.1982G=
NR_148400.2:n.1581G=