Canonical Allele Identifier: CA1881760613
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523104T= , CM000671.2:g.131523104T= GRCh38
NC_000009.11:g.134398491T= , CM000671.1:g.134398491T= GRCh37
NC_000009.10:g.133388312T= NCBI36
NG_008896.1:g.25203T=
NG_008896.2:g.25203T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.2014T= ENSP00000343034.7:p.Ter672=
ENST00000404875.7:n.2716T=
ENST00000423007.6:c.2233T= ENSP00000404119.2:p.Ter745=
ENST00000677295.2:c.*2520T= ENSP00000504346.2:n.*2520T=
ENST00000678264.2:c.*2359T= ENSP00000503157.2:n.*2359T=
ENST00000682070.1:n.2486T=
ENST00000682639.1:c.173T=
ENST00000682813.1:n.2573T=
ENST00000683231.1:c.173T=
ENST00000683392.1:n.4768T=
ENST00000683712.1:n.2581T=
ENST00000683900.1:n.4076T=
ENST00000684062.1:n.2842T=
ENST00000684399.1:c.173T=
ENST00000684579.1:n.4022T=
ENST00000341012.12:c.2014T= ENSP00000343034.7:p.Ter672=
ENST00000372220.5:c.1045T= ENSP00000361294.5:p.Ter349=
ENST00000372228.9:c.2242T= ENSP00000361302.3:p.Ter748=
ENST00000402686.8:c.2176T= MANE Select ENSP00000385797.4:p.Ter726=
ENST00000676640.1:c.2176T= ENSP00000503281.1:p.Ter726=
ENST00000676803.1:c.1237T= ENSP00000503093.1:p.Ter413=
ENST00000676835.1:c.*1391T= ENSP00000502911.1:n.*1391T=
ENST00000677029.1:c.1720T= ENSP00000502936.1:p.Ter574=
ENST00000677099.1:c.*1886T= ENSP00000504553.1:n.*1886T=
ENST00000677216.1:c.1825T= ENSP00000503772.1:p.Ter609=
ENST00000677295.1:c.*1398T= ENSP00000504346.1:n.*1398T=
ENST00000677444.1:c.2121T=
ENST00000677586.1:n.1543T=
ENST00000677626.1:c.1825T= ENSP00000503552.1:p.Ter609=
ENST00000677853.1:c.*1184T= ENSP00000503488.1:n.*1184T=
ENST00000678264.1:c.*1553T= ENSP00000503157.1:n.*1553T=
ENST00000678303.1:c.2086T= ENSP00000503696.1:p.Ter696=
ENST00000678366.1:c.*2425T= ENSP00000504353.1:n.*2425T=
ENST00000678546.1:c.*2121T= ENSP00000503062.1:n.*2121T=
ENST00000678548.1:c.*2315T= ENSP00000503934.1:n.*2315T=
ENST00000678626.1:n.2012T=
ENST00000678739.1:c.*2342T= ENSP00000503806.1:n.*2342T=
ENST00000678833.1:c.*1928T= ENSP00000503893.1:n.*1928T=
ENST00000679023.1:c.2014T= ENSP00000503718.1:p.Ter672=
ENST00000679076.1:c.1795T=
ENST00000679111.1:c.*932T= ENSP00000504257.1:n.*932T=
ENST00000679189.1:c.1825T= ENSP00000503356.1:p.Ter609=
ENST00000341012.11:c.2014T= ENSP00000343034.7:p.Ter672=
ENST00000372220.4:c.1039T= ENSP00000361294.4:p.Ter347=
ENST00000372228.7:c.2242T= ENSP00000361302.3:p.Ter748=
ENST00000402686.7:c.2176T= ENSP00000385797.3:p.Ter726=
ENST00000404875.6:c.1825T= ENSP00000384531.2:p.Ter609=
ENST00000423007.5:c.2176T= ENSP00000404119.1:p.Ter726=
ENST00000485278.5:n.2726T=
NM_001077365.1:c.2176T= NP_001070833.1:p.Ter726=
NM_001077366.1:c.2014T= NP_001070834.1:p.Ter672=
NM_001136113.1:c.2176T= NP_001129585.1:p.Ter726=
NM_001136114.1:c.1825T= NP_001129586.1:p.Ter609=
NM_007171.3:c.2242T= NP_009102.3:p.Ter748=
XM_005272156.1:c.2242T= XP_005272213.1:p.Ter748=
XM_005272158.1:c.2080T= XP_005272215.1:p.Ter694=
XM_005272159.1:c.1891T= XP_005272216.1:p.Ter631=
XM_005272162.1:c.1045T= XP_005272219.1:p.Ter349=
XM_006716932.1:c.1891T= XP_006716995.1:p.Ter631=
XM_011518140.1:c.2095T= XP_011516442.1:p.Ter699=
XM_011518141.1:c.2029T= XP_011516443.1:p.Ter677=
XM_011518142.1:c.1933T= XP_011516444.1:p.Ter645=
XM_011518143.1:c.1927T= XP_011516445.1:p.Ter643=
XM_011518145.1:c.1786T= XP_011516447.1:p.Ter596=
XM_011518147.1:c.1114T= XP_011516449.1:p.Ter372=
XR_929703.1:n.2418T=
NM_001353193.1:c.2242T= NP_001340122.1:p.Ter748=
NM_001353194.1:c.2014T= NP_001340123.1:p.Ter672=
NM_001353195.1:c.1825T= NP_001340124.1:p.Ter609=
NM_001353196.1:c.2086T= NP_001340125.1:p.Ter696=
NM_001353197.1:c.2080T= NP_001340126.1:p.Ter694=
NM_001353198.1:c.2080T= NP_001340127.1:p.Ter694=
NM_001353199.1:c.1891T= NP_001340128.1:p.Ter631=
NM_001353200.1:c.1720T= NP_001340129.1:p.Ter574=
NR_148391.1:n.2226T=
NR_148392.1:n.2444T=
NR_148393.1:n.2365T=
NR_148394.1:n.2119T=
NR_148395.1:n.2517T=
NR_148396.1:n.2151T=
NR_148397.1:n.2276T=
NR_148398.1:n.2231T=
NR_148399.1:n.2757T=
NR_148400.1:n.2356T=
XM_005272162.3:c.1045T= XP_005272219.1:p.Ter349=
XM_006716932.2:c.1891T= XP_006716995.1:p.Ter631=
XM_011518140.2:c.2095T= XP_011516442.1:p.Ter699=
XM_011518141.2:c.2029T= XP_011516443.1:p.Ter677=
XM_011518142.2:c.1933T= XP_011516444.1:p.Ter645=
XM_011518143.2:c.1927T= XP_011516445.1:p.Ter643=
XM_011518145.2:c.1786T= XP_011516447.1:p.Ter596=
XM_017014205.2:c.1045T= XP_016869694.1:p.Ter349=
XM_024447380.1:c.1045T= XP_024303148.1:p.Ter349=
XM_024447381.1:c.1351T= XP_024303149.1:p.Ter451=
XM_024447382.1:c.1045T= XP_024303150.1:p.Ter349=
XR_001746160.2:n.2346T=
XR_001746162.2:n.2551T=
XR_001746164.1:n.2268T=
XR_001746166.2:n.2563T=
NM_001077365.2:c.2176T= MANE Select NP_001070833.1:p.Ter726=
NM_001077366.2:c.2014T= NP_001070834.1:p.Ter672=
NM_001136113.2:c.2176T= NP_001129585.1:p.Ter726=
NM_001136114.2:c.1825T= NP_001129586.1:p.Ter609=
NM_001353193.2:c.2242T= NP_001340122.2:p.Ter748=
NM_001353194.2:c.2014T= NP_001340123.1:p.Ter672=
NM_001353195.2:c.1825T= NP_001340124.1:p.Ter609=
NM_001353196.2:c.2086T= NP_001340125.1:p.Ter696=
NM_001353197.2:c.2080T= NP_001340126.2:p.Ter694=
NM_001353198.2:c.2080T= NP_001340127.2:p.Ter694=
NM_001353199.2:c.1891T= NP_001340128.2:p.Ter631=
NM_001353200.2:c.1720T= NP_001340129.1:p.Ter574=
NM_001374689.1:c.2164T= NP_001361618.1:p.Ter722=
NM_001374690.1:c.1957T= NP_001361619.1:p.Ter653=
NM_001374691.1:c.1825T= NP_001361620.1:p.Ter609=
NM_001374692.1:c.1825T= NP_001361621.1:p.Ter609=
NM_001374693.1:c.1825T= NP_001361622.1:p.Ter609=
NM_001374695.1:c.1786T= NP_001361624.1:p.Ter596=
NM_007171.4:c.2242T= NP_009102.4:p.Ter748=
NR_148391.2:n.2210T=
NR_148392.2:n.2428T=
NR_148393.2:n.2349T=
NR_148394.2:n.2103T=
NR_148395.2:n.2501T=
NR_148396.2:n.2135T=
NR_148397.2:n.2260T=
NR_148398.2:n.2215T=
NR_148399.2:n.2741T=
NR_148400.2:n.2340T=