Canonical Allele Identifier: CA1881751915
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518515T= , CM000671.2:g.131518515T= GRCh38
NC_000009.11:g.134393902T= , CM000671.1:g.134393902T= GRCh37
NC_000009.10:g.133383723T= NCBI36
NG_008896.1:g.20614T=
NG_008896.2:g.20614T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1181T= ENSP00000343034.7:p.Val394=
ENST00000404875.7:n.1883T=
ENST00000423007.6:c.1400T= ENSP00000404119.2:p.Val467=
ENST00000677295.2:c.*1687T= ENSP00000504346.2:n.*1687T=
ENST00000678264.2:c.*1526T= ENSP00000503157.2:n.*1526T=
ENST00000682070.1:n.1808T=
ENST00000682535.1:n.115T=
ENST00000682539.1:c.281T=
ENST00000682813.1:n.1608T=
ENST00000683110.1:n.71T=
ENST00000683392.1:n.4090T=
ENST00000683712.1:n.1748T=
ENST00000683900.1:n.3243T=
ENST00000684062.1:n.2009T=
ENST00000684579.1:n.3189T=
ENST00000684679.1:n.570T=
ENST00000341012.12:c.1181T= ENSP00000343034.7:p.Val394=
ENST00000372220.5:c.212T= ENSP00000361294.5:p.Val71=
ENST00000372228.9:c.1409T= ENSP00000361302.3:p.Val470=
ENST00000402686.8:c.1343T= MANE Select ENSP00000385797.4:p.Val448=
ENST00000676640.1:c.1343T= ENSP00000503281.1:p.Val448=
ENST00000676803.1:c.518T= ENSP00000503093.1:p.Val173=
ENST00000676835.1:c.*558T= ENSP00000502911.1:n.*558T=
ENST00000677029.1:c.887T= ENSP00000502936.1:p.Val296=
ENST00000677099.1:c.*1053T= ENSP00000504553.1:n.*1053T=
ENST00000677216.1:c.992T= ENSP00000503772.1:p.Val331=
ENST00000677221.1:n.368T=
ENST00000677295.1:c.*720T= ENSP00000504346.1:n.*720T=
ENST00000677444.1:c.1149T=
ENST00000677586.1:n.824T=
ENST00000677626.1:c.992T= ENSP00000503552.1:p.Val331=
ENST00000677677.1:n.1303T=
ENST00000677853.1:c.*351T= ENSP00000503488.1:n.*351T=
ENST00000677983.1:n.432T=
ENST00000678202.1:n.363T=
ENST00000678264.1:c.*720T= ENSP00000503157.1:n.*720T=
ENST00000678303.1:c.1253T= ENSP00000503696.1:p.Val418=
ENST00000678366.1:c.*1592T= ENSP00000504353.1:n.*1592T=
ENST00000678546.1:c.*1288T= ENSP00000503062.1:n.*1288T=
ENST00000678548.1:c.*1415T= ENSP00000503934.1:n.*1415T=
ENST00000678626.1:n.1040T=
ENST00000678733.1:c.424T=
ENST00000678739.1:c.*1669T= ENSP00000503806.1:n.*1669T=
ENST00000678795.1:n.430T=
ENST00000678833.1:c.*790T= ENSP00000503893.1:n.*790T=
ENST00000678942.1:c.523T= ENSP00000504690.1:n.523T=
ENST00000679023.1:c.1181T= ENSP00000503718.1:p.Val394=
ENST00000679076.1:c.962T=
ENST00000679111.1:c.1343T= ENSP00000504257.1:p.Val448=
ENST00000679189.1:c.992T= ENSP00000503356.1:p.Val331=
ENST00000341012.11:c.1181T= ENSP00000343034.7:p.Val394=
ENST00000372220.4:c.206T= ENSP00000361294.4:p.Val69=
ENST00000372228.7:c.1409T= ENSP00000361302.3:p.Val470=
ENST00000402686.7:c.1343T= ENSP00000385797.3:p.Val448=
ENST00000404875.6:c.992T= ENSP00000384531.2:p.Val331=
ENST00000423007.5:c.1343T= ENSP00000404119.1:p.Val448=
ENST00000485278.5:n.1898T=
NM_001077365.1:c.1343T= NP_001070833.1:p.Val448=
NM_001077366.1:c.1181T= NP_001070834.1:p.Val394=
NM_001136113.1:c.1343T= NP_001129585.1:p.Val448=
NM_001136114.1:c.992T= NP_001129586.1:p.Val331=
NM_007171.3:c.1409T= NP_009102.3:p.Val470=
XM_005272156.1:c.1409T= XP_005272213.1:p.Val470=
XM_005272158.1:c.1247T= XP_005272215.1:p.Val416=
XM_005272159.1:c.1058T= XP_005272216.1:p.Val353=
XM_005272162.1:c.212T= XP_005272219.1:p.Val71=
XM_006716932.1:c.1058T= XP_006716995.1:p.Val353=
XM_011518140.1:c.1262T= XP_011516442.1:p.Val421=
XM_011518141.1:c.1196T= XP_011516443.1:p.Val399=
XM_011518142.1:c.1100T= XP_011516444.1:p.Val367=
XM_011518143.1:c.1094T= XP_011516445.1:p.Val365=
XM_011518144.1:c.1409T= XP_011516446.1:p.Val470=
XM_011518145.1:c.953T= XP_011516447.1:p.Val318=
XM_011518146.1:c.1094T= XP_011516448.1:p.Val365=
XM_011518147.1:c.281T= XP_011516449.1:p.Val94=
XR_929703.1:n.1585T=
NM_001353193.1:c.1409T= NP_001340122.1:p.Val470=
NM_001353194.1:c.1181T= NP_001340123.1:p.Val394=
NM_001353195.1:c.992T= NP_001340124.1:p.Val331=
NM_001353196.1:c.1253T= NP_001340125.1:p.Val418=
NM_001353197.1:c.1247T= NP_001340126.1:p.Val416=
NM_001353198.1:c.1247T= NP_001340127.1:p.Val416=
NM_001353199.1:c.1058T= NP_001340128.1:p.Val353=
NM_001353200.1:c.887T= NP_001340129.1:p.Val296=
NR_148391.1:n.1393T=
NR_148392.1:n.1611T=
NR_148393.1:n.1393T=
NR_148394.1:n.1286T=
NR_148395.1:n.1545T=
NR_148396.1:n.1179T=
NR_148397.1:n.1443T=
NR_148398.1:n.1398T=
NR_148399.1:n.1785T=
NR_148400.1:n.1384T=
XM_005272162.3:c.212T= XP_005272219.1:p.Val71=
XM_006716932.2:c.1058T= XP_006716995.1:p.Val353=
XM_011518140.2:c.1262T= XP_011516442.1:p.Val421=
XM_011518141.2:c.1196T= XP_011516443.1:p.Val399=
XM_011518142.2:c.1100T= XP_011516444.1:p.Val367=
XM_011518143.2:c.1094T= XP_011516445.1:p.Val365=
XM_011518145.2:c.953T= XP_011516447.1:p.Val318=
XM_017014205.2:c.212T= XP_016869694.1:p.Val71=
XM_024447380.1:c.212T= XP_024303148.1:p.Val71=
XM_024447381.1:c.518T= XP_024303149.1:p.Val173=
XM_024447382.1:c.212T= XP_024303150.1:p.Val71=
XR_001746160.2:n.1513T=
XR_001746162.2:n.1579T=
XR_001746164.1:n.1296T=
XR_001746166.2:n.1730T=
NM_001077365.2:c.1343T= MANE Select NP_001070833.1:p.Val448=
NM_001077366.2:c.1181T= NP_001070834.1:p.Val394=
NM_001136113.2:c.1343T= NP_001129585.1:p.Val448=
NM_001136114.2:c.992T= NP_001129586.1:p.Val331=
NM_001353193.2:c.1409T= NP_001340122.2:p.Val470=
NM_001353194.2:c.1181T= NP_001340123.1:p.Val394=
NM_001353195.2:c.992T= NP_001340124.1:p.Val331=
NM_001353196.2:c.1253T= NP_001340125.1:p.Val418=
NM_001353197.2:c.1247T= NP_001340126.2:p.Val416=
NM_001353198.2:c.1247T= NP_001340127.2:p.Val416=
NM_001353199.2:c.1058T= NP_001340128.2:p.Val353=
NM_001353200.2:c.887T= NP_001340129.1:p.Val296=
NM_001374689.1:c.1331T= NP_001361618.1:p.Val444=
NM_001374690.1:c.1343T= NP_001361619.1:p.Val448=
NM_001374691.1:c.992T= NP_001361620.1:p.Val331=
NM_001374692.1:c.992T= NP_001361621.1:p.Val331=
NM_001374693.1:c.992T= NP_001361622.1:p.Val331=
NM_001374695.1:c.953T= NP_001361624.1:p.Val318=
NM_007171.4:c.1409T= NP_009102.4:p.Val470=
NR_148391.2:n.1377T=
NR_148392.2:n.1595T=
NR_148393.2:n.1377T=
NR_148394.2:n.1270T=
NR_148395.2:n.1529T=
NR_148396.2:n.1163T=
NR_148397.2:n.1427T=
NR_148398.2:n.1382T=
NR_148399.2:n.1769T=
NR_148400.2:n.1368T=