Canonical Allele Identifier: CA1881751851
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518487A= , CM000671.2:g.131518487A= GRCh38
NC_000009.11:g.134393874A= , CM000671.1:g.134393874A= GRCh37
NC_000009.10:g.133383695A= NCBI36
NG_008896.1:g.20586A=
NG_008896.2:g.20586A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1153A= ENSP00000343034.7:p.Ile385=
ENST00000404875.7:n.1855A=
ENST00000423007.6:c.1372A= ENSP00000404119.2:p.Ile458=
ENST00000677295.2:c.*1659A= ENSP00000504346.2:n.*1659A=
ENST00000678264.2:c.*1498A= ENSP00000503157.2:n.*1498A=
ENST00000682070.1:n.1780A=
ENST00000682535.1:n.87A=
ENST00000682539.1:c.253A=
ENST00000682813.1:n.1580A=
ENST00000683110.1:n.43A=
ENST00000683392.1:n.4062A=
ENST00000683712.1:n.1720A=
ENST00000683900.1:n.3215A=
ENST00000684062.1:n.1981A=
ENST00000684579.1:n.3161A=
ENST00000684679.1:n.542A=
ENST00000341012.12:c.1153A= ENSP00000343034.7:p.Ile385=
ENST00000372220.5:c.184A= ENSP00000361294.5:p.Ile62=
ENST00000372228.9:c.1381A= ENSP00000361302.3:p.Ile461=
ENST00000402686.8:c.1315A= MANE Select ENSP00000385797.4:p.Ile439=
ENST00000676640.1:c.1315A= ENSP00000503281.1:p.Ile439=
ENST00000676803.1:c.490A= ENSP00000503093.1:p.Ile164=
ENST00000676835.1:c.*530A= ENSP00000502911.1:n.*530A=
ENST00000677029.1:c.859A= ENSP00000502936.1:p.Ile287=
ENST00000677099.1:c.*1025A= ENSP00000504553.1:n.*1025A=
ENST00000677216.1:c.964A= ENSP00000503772.1:p.Ile322=
ENST00000677221.1:n.340A=
ENST00000677295.1:c.*692A= ENSP00000504346.1:n.*692A=
ENST00000677444.1:c.1121A=
ENST00000677586.1:n.796A=
ENST00000677626.1:c.964A= ENSP00000503552.1:p.Ile322=
ENST00000677677.1:n.1275A=
ENST00000677853.1:c.*323A= ENSP00000503488.1:n.*323A=
ENST00000677983.1:n.404A=
ENST00000678202.1:n.335A=
ENST00000678264.1:c.*692A= ENSP00000503157.1:n.*692A=
ENST00000678303.1:c.1225A= ENSP00000503696.1:p.Ile409=
ENST00000678366.1:c.*1564A= ENSP00000504353.1:n.*1564A=
ENST00000678546.1:c.*1260A= ENSP00000503062.1:n.*1260A=
ENST00000678548.1:c.*1387A= ENSP00000503934.1:n.*1387A=
ENST00000678626.1:n.1012A=
ENST00000678733.1:c.396A=
ENST00000678739.1:c.*1641A= ENSP00000503806.1:n.*1641A=
ENST00000678795.1:n.402A=
ENST00000678833.1:c.*762A= ENSP00000503893.1:n.*762A=
ENST00000678942.1:c.495A= ENSP00000504690.1:n.495A=
ENST00000679023.1:c.1153A= ENSP00000503718.1:p.Ile385=
ENST00000679076.1:c.934A=
ENST00000679111.1:c.1315A= ENSP00000504257.1:p.Ile439=
ENST00000679189.1:c.964A= ENSP00000503356.1:p.Ile322=
ENST00000341012.11:c.1153A= ENSP00000343034.7:p.Ile385=
ENST00000372220.4:c.178A= ENSP00000361294.4:p.Ile60=
ENST00000372228.7:c.1381A= ENSP00000361302.3:p.Ile461=
ENST00000402686.7:c.1315A= ENSP00000385797.3:p.Ile439=
ENST00000404875.6:c.964A= ENSP00000384531.2:p.Ile322=
ENST00000423007.5:c.1315A= ENSP00000404119.1:p.Ile439=
ENST00000485278.5:n.1870A=
NM_001077365.1:c.1315A= NP_001070833.1:p.Ile439=
NM_001077366.1:c.1153A= NP_001070834.1:p.Ile385=
NM_001136113.1:c.1315A= NP_001129585.1:p.Ile439=
NM_001136114.1:c.964A= NP_001129586.1:p.Ile322=
NM_007171.3:c.1381A= NP_009102.3:p.Ile461=
XM_005272156.1:c.1381A= XP_005272213.1:p.Ile461=
XM_005272158.1:c.1219A= XP_005272215.1:p.Ile407=
XM_005272159.1:c.1030A= XP_005272216.1:p.Ile344=
XM_005272162.1:c.184A= XP_005272219.1:p.Ile62=
XM_006716932.1:c.1030A= XP_006716995.1:p.Ile344=
XM_011518140.1:c.1234A= XP_011516442.1:p.Ile412=
XM_011518141.1:c.1168A= XP_011516443.1:p.Ile390=
XM_011518142.1:c.1072A= XP_011516444.1:p.Ile358=
XM_011518143.1:c.1066A= XP_011516445.1:p.Ile356=
XM_011518144.1:c.1381A= XP_011516446.1:p.Ile461=
XM_011518145.1:c.925A= XP_011516447.1:p.Ile309=
XM_011518146.1:c.1066A= XP_011516448.1:p.Ile356=
XM_011518147.1:c.253A= XP_011516449.1:p.Ile85=
XR_929703.1:n.1557A=
NM_001353193.1:c.1381A= NP_001340122.1:p.Ile461=
NM_001353194.1:c.1153A= NP_001340123.1:p.Ile385=
NM_001353195.1:c.964A= NP_001340124.1:p.Ile322=
NM_001353196.1:c.1225A= NP_001340125.1:p.Ile409=
NM_001353197.1:c.1219A= NP_001340126.1:p.Ile407=
NM_001353198.1:c.1219A= NP_001340127.1:p.Ile407=
NM_001353199.1:c.1030A= NP_001340128.1:p.Ile344=
NM_001353200.1:c.859A= NP_001340129.1:p.Ile287=
NR_148391.1:n.1365A=
NR_148392.1:n.1583A=
NR_148393.1:n.1365A=
NR_148394.1:n.1258A=
NR_148395.1:n.1517A=
NR_148396.1:n.1151A=
NR_148397.1:n.1415A=
NR_148398.1:n.1370A=
NR_148399.1:n.1757A=
NR_148400.1:n.1356A=
XM_005272162.3:c.184A= XP_005272219.1:p.Ile62=
XM_006716932.2:c.1030A= XP_006716995.1:p.Ile344=
XM_011518140.2:c.1234A= XP_011516442.1:p.Ile412=
XM_011518141.2:c.1168A= XP_011516443.1:p.Ile390=
XM_011518142.2:c.1072A= XP_011516444.1:p.Ile358=
XM_011518143.2:c.1066A= XP_011516445.1:p.Ile356=
XM_011518145.2:c.925A= XP_011516447.1:p.Ile309=
XM_017014205.2:c.184A= XP_016869694.1:p.Ile62=
XM_024447380.1:c.184A= XP_024303148.1:p.Ile62=
XM_024447381.1:c.490A= XP_024303149.1:p.Ile164=
XM_024447382.1:c.184A= XP_024303150.1:p.Ile62=
XR_001746160.2:n.1485A=
XR_001746162.2:n.1551A=
XR_001746164.1:n.1268A=
XR_001746166.2:n.1702A=
NM_001077365.2:c.1315A= MANE Select NP_001070833.1:p.Ile439=
NM_001077366.2:c.1153A= NP_001070834.1:p.Ile385=
NM_001136113.2:c.1315A= NP_001129585.1:p.Ile439=
NM_001136114.2:c.964A= NP_001129586.1:p.Ile322=
NM_001353193.2:c.1381A= NP_001340122.2:p.Ile461=
NM_001353194.2:c.1153A= NP_001340123.1:p.Ile385=
NM_001353195.2:c.964A= NP_001340124.1:p.Ile322=
NM_001353196.2:c.1225A= NP_001340125.1:p.Ile409=
NM_001353197.2:c.1219A= NP_001340126.2:p.Ile407=
NM_001353198.2:c.1219A= NP_001340127.2:p.Ile407=
NM_001353199.2:c.1030A= NP_001340128.2:p.Ile344=
NM_001353200.2:c.859A= NP_001340129.1:p.Ile287=
NM_001374689.1:c.1303A= NP_001361618.1:p.Ile435=
NM_001374690.1:c.1315A= NP_001361619.1:p.Ile439=
NM_001374691.1:c.964A= NP_001361620.1:p.Ile322=
NM_001374692.1:c.964A= NP_001361621.1:p.Ile322=
NM_001374693.1:c.964A= NP_001361622.1:p.Ile322=
NM_001374695.1:c.925A= NP_001361624.1:p.Ile309=
NM_007171.4:c.1381A= NP_009102.4:p.Ile461=
NR_148391.2:n.1349A=
NR_148392.2:n.1567A=
NR_148393.2:n.1349A=
NR_148394.2:n.1242A=
NR_148395.2:n.1501A=
NR_148396.2:n.1135A=
NR_148397.2:n.1399A=
NR_148398.2:n.1354A=
NR_148399.2:n.1741A=
NR_148400.2:n.1340A=