Canonical Allele Identifier: CA1881752807
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518943A= , CM000671.2:g.131518943A= GRCh38
NC_000009.11:g.134394330A= , CM000671.1:g.134394330A= GRCh37
NC_000009.10:g.133384151A= NCBI36
NG_008896.1:g.21042A=
NG_008896.2:g.21042A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1310A= ENSP00000343034.7:p.His437=
ENST00000404875.7:n.2012A=
ENST00000423007.6:c.1529A= ENSP00000404119.2:p.His510=
ENST00000677295.2:c.*1816A= ENSP00000504346.2:n.*1816A=
ENST00000678264.2:c.*1655A= ENSP00000503157.2:n.*1655A=
ENST00000682070.1:n.1937A=
ENST00000682539.1:c.410A=
ENST00000682813.1:n.1876A=
ENST00000683392.1:n.4219A=
ENST00000683712.1:n.1877A=
ENST00000683900.1:n.3372A=
ENST00000684062.1:n.2138A=
ENST00000684579.1:n.3318A=
ENST00000684679.1:n.699A=
ENST00000341012.12:c.1310A= ENSP00000343034.7:p.His437=
ENST00000372220.5:c.341A= ENSP00000361294.5:p.His114=
ENST00000372228.9:c.1538A= ENSP00000361302.3:p.His513=
ENST00000402686.8:c.1472A= MANE Select ENSP00000385797.4:p.His491=
ENST00000676640.1:c.1472A= ENSP00000503281.1:p.His491=
ENST00000676803.1:c.647A= ENSP00000503093.1:p.His216=
ENST00000676835.1:c.*687A= ENSP00000502911.1:n.*687A=
ENST00000677029.1:c.1016A= ENSP00000502936.1:p.His339=
ENST00000677099.1:c.*1182A= ENSP00000504553.1:n.*1182A=
ENST00000677216.1:c.1121A= ENSP00000503772.1:p.His374=
ENST00000677221.1:n.497A=
ENST00000677295.1:c.*849A= ENSP00000504346.1:n.*849A=
ENST00000677444.1:c.1417A=
ENST00000677586.1:n.953A=
ENST00000677626.1:c.1121A= ENSP00000503552.1:p.His374=
ENST00000677677.1:n.1432A=
ENST00000677853.1:c.*480A= ENSP00000503488.1:n.*480A=
ENST00000678202.1:n.631A=
ENST00000678264.1:c.*849A= ENSP00000503157.1:n.*849A=
ENST00000678303.1:c.1382A= ENSP00000503696.1:p.His461=
ENST00000678366.1:c.*1721A= ENSP00000504353.1:n.*1721A=
ENST00000678546.1:c.*1417A= ENSP00000503062.1:n.*1417A=
ENST00000678548.1:c.*1544A= ENSP00000503934.1:n.*1544A=
ENST00000678626.1:n.1308A=
ENST00000678733.1:c.553A=
ENST00000678739.1:c.*1798A= ENSP00000503806.1:n.*1798A=
ENST00000678833.1:c.*919A= ENSP00000503893.1:n.*919A=
ENST00000679023.1:c.1310A= ENSP00000503718.1:p.His437=
ENST00000679076.1:c.1091A=
ENST00000679111.1:c.*228A= ENSP00000504257.1:n.*228A=
ENST00000679189.1:c.1121A= ENSP00000503356.1:p.His374=
ENST00000341012.11:c.1310A= ENSP00000343034.7:p.His437=
ENST00000372220.4:c.335A= ENSP00000361294.4:p.His112=
ENST00000372228.7:c.1538A= ENSP00000361302.3:p.His513=
ENST00000402686.7:c.1472A= ENSP00000385797.3:p.His491=
ENST00000404875.6:c.1121A= ENSP00000384531.2:p.His374=
ENST00000423007.5:c.1472A= ENSP00000404119.1:p.His491=
ENST00000467848.1:n.176A=
ENST00000485278.5:n.2027A=
NM_001077365.1:c.1472A= NP_001070833.1:p.His491=
NM_001077366.1:c.1310A= NP_001070834.1:p.His437=
NM_001136113.1:c.1472A= NP_001129585.1:p.His491=
NM_001136114.1:c.1121A= NP_001129586.1:p.His374=
NM_007171.3:c.1538A= NP_009102.3:p.His513=
XM_005272156.1:c.1538A= XP_005272213.1:p.His513=
XM_005272158.1:c.1376A= XP_005272215.1:p.His459=
XM_005272159.1:c.1187A= XP_005272216.1:p.His396=
XM_005272162.1:c.341A= XP_005272219.1:p.His114=
XM_006716932.1:c.1187A= XP_006716995.1:p.His396=
XM_011518140.1:c.1391A= XP_011516442.1:p.His464=
XM_011518141.1:c.1325A= XP_011516443.1:p.His442=
XM_011518142.1:c.1229A= XP_011516444.1:p.His410=
XM_011518143.1:c.1223A= XP_011516445.1:p.His408=
XM_011518145.1:c.1082A= XP_011516447.1:p.His361=
XM_011518147.1:c.410A= XP_011516449.1:p.His137=
XR_929703.1:n.1714A=
NM_001353193.1:c.1538A= NP_001340122.1:p.His513=
NM_001353194.1:c.1310A= NP_001340123.1:p.His437=
NM_001353195.1:c.1121A= NP_001340124.1:p.His374=
NM_001353196.1:c.1382A= NP_001340125.1:p.His461=
NM_001353197.1:c.1376A= NP_001340126.1:p.His459=
NM_001353198.1:c.1376A= NP_001340127.1:p.His459=
NM_001353199.1:c.1187A= NP_001340128.1:p.His396=
NM_001353200.1:c.1016A= NP_001340129.1:p.His339=
NR_148391.1:n.1522A=
NR_148392.1:n.1740A=
NR_148393.1:n.1661A=
NR_148394.1:n.1415A=
NR_148395.1:n.1813A=
NR_148396.1:n.1447A=
NR_148397.1:n.1572A=
NR_148398.1:n.1527A=
NR_148399.1:n.2053A=
NR_148400.1:n.1652A=
XM_005272162.3:c.341A= XP_005272219.1:p.His114=
XM_006716932.2:c.1187A= XP_006716995.1:p.His396=
XM_011518140.2:c.1391A= XP_011516442.1:p.His464=
XM_011518141.2:c.1325A= XP_011516443.1:p.His442=
XM_011518142.2:c.1229A= XP_011516444.1:p.His410=
XM_011518143.2:c.1223A= XP_011516445.1:p.His408=
XM_011518145.2:c.1082A= XP_011516447.1:p.His361=
XM_017014205.2:c.341A= XP_016869694.1:p.His114=
XM_024447380.1:c.341A= XP_024303148.1:p.His114=
XM_024447381.1:c.647A= XP_024303149.1:p.His216=
XM_024447382.1:c.341A= XP_024303150.1:p.His114=
XR_001746160.2:n.1642A=
XR_001746162.2:n.1847A=
XR_001746164.1:n.1564A=
XR_001746166.2:n.1859A=
NM_001077365.2:c.1472A= MANE Select NP_001070833.1:p.His491=
NM_001077366.2:c.1310A= NP_001070834.1:p.His437=
NM_001136113.2:c.1472A= NP_001129585.1:p.His491=
NM_001136114.2:c.1121A= NP_001129586.1:p.His374=
NM_001353193.2:c.1538A= NP_001340122.2:p.His513=
NM_001353194.2:c.1310A= NP_001340123.1:p.His437=
NM_001353195.2:c.1121A= NP_001340124.1:p.His374=
NM_001353196.2:c.1382A= NP_001340125.1:p.His461=
NM_001353197.2:c.1376A= NP_001340126.2:p.His459=
NM_001353198.2:c.1376A= NP_001340127.2:p.His459=
NM_001353199.2:c.1187A= NP_001340128.2:p.His396=
NM_001353200.2:c.1016A= NP_001340129.1:p.His339=
NM_001374689.1:c.1460A= NP_001361618.1:p.His487=
NM_001374690.1:c.1365+406A= NP_001361619.1:n.1365+406A=
NM_001374691.1:c.1121A= NP_001361620.1:p.His374=
NM_001374692.1:c.1121A= NP_001361621.1:p.His374=
NM_001374693.1:c.1121A= NP_001361622.1:p.His374=
NM_001374695.1:c.1082A= NP_001361624.1:p.His361=
NM_007171.4:c.1538A= NP_009102.4:p.His513=
NR_148391.2:n.1506A=
NR_148392.2:n.1724A=
NR_148393.2:n.1645A=
NR_148394.2:n.1399A=
NR_148395.2:n.1797A=
NR_148396.2:n.1431A=
NR_148397.2:n.1556A=
NR_148398.2:n.1511A=
NR_148399.2:n.2037A=
NR_148400.2:n.1636A=