Canonical Allele Identifier: CA1881751874
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518500T= , CM000671.2:g.131518500T= GRCh38
NC_000009.11:g.134393887T= , CM000671.1:g.134393887T= GRCh37
NC_000009.10:g.133383708T= NCBI36
NG_008896.1:g.20599T=
NG_008896.2:g.20599T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1166T= ENSP00000343034.7:p.Val389=
ENST00000404875.7:n.1868T=
ENST00000423007.6:c.1385T= ENSP00000404119.2:p.Val462=
ENST00000677295.2:c.*1672T= ENSP00000504346.2:n.*1672T=
ENST00000678264.2:c.*1511T= ENSP00000503157.2:n.*1511T=
ENST00000682070.1:n.1793T=
ENST00000682535.1:n.100T=
ENST00000682539.1:c.266T=
ENST00000682813.1:n.1593T=
ENST00000683110.1:n.56T=
ENST00000683392.1:n.4075T=
ENST00000683712.1:n.1733T=
ENST00000683900.1:n.3228T=
ENST00000684062.1:n.1994T=
ENST00000684579.1:n.3174T=
ENST00000684679.1:n.555T=
ENST00000341012.12:c.1166T= ENSP00000343034.7:p.Val389=
ENST00000372220.5:c.197T= ENSP00000361294.5:p.Val66=
ENST00000372228.9:c.1394T= ENSP00000361302.3:p.Val465=
ENST00000402686.8:c.1328T= MANE Select ENSP00000385797.4:p.Val443=
ENST00000676640.1:c.1328T= ENSP00000503281.1:p.Val443=
ENST00000676803.1:c.503T= ENSP00000503093.1:p.Val168=
ENST00000676835.1:c.*543T= ENSP00000502911.1:n.*543T=
ENST00000677029.1:c.872T= ENSP00000502936.1:p.Val291=
ENST00000677099.1:c.*1038T= ENSP00000504553.1:n.*1038T=
ENST00000677216.1:c.977T= ENSP00000503772.1:p.Val326=
ENST00000677221.1:n.353T=
ENST00000677295.1:c.*705T= ENSP00000504346.1:n.*705T=
ENST00000677444.1:c.1134T=
ENST00000677586.1:n.809T=
ENST00000677626.1:c.977T= ENSP00000503552.1:p.Val326=
ENST00000677677.1:n.1288T=
ENST00000677853.1:c.*336T= ENSP00000503488.1:n.*336T=
ENST00000677983.1:n.417T=
ENST00000678202.1:n.348T=
ENST00000678264.1:c.*705T= ENSP00000503157.1:n.*705T=
ENST00000678303.1:c.1238T= ENSP00000503696.1:p.Val413=
ENST00000678366.1:c.*1577T= ENSP00000504353.1:n.*1577T=
ENST00000678546.1:c.*1273T= ENSP00000503062.1:n.*1273T=
ENST00000678548.1:c.*1400T= ENSP00000503934.1:n.*1400T=
ENST00000678626.1:n.1025T=
ENST00000678733.1:c.409T=
ENST00000678739.1:c.*1654T= ENSP00000503806.1:n.*1654T=
ENST00000678795.1:n.415T=
ENST00000678833.1:c.*775T= ENSP00000503893.1:n.*775T=
ENST00000678942.1:c.508T= ENSP00000504690.1:n.508T=
ENST00000679023.1:c.1166T= ENSP00000503718.1:p.Val389=
ENST00000679076.1:c.947T=
ENST00000679111.1:c.1328T= ENSP00000504257.1:p.Val443=
ENST00000679189.1:c.977T= ENSP00000503356.1:p.Val326=
ENST00000341012.11:c.1166T= ENSP00000343034.7:p.Val389=
ENST00000372220.4:c.191T= ENSP00000361294.4:p.Val64=
ENST00000372228.7:c.1394T= ENSP00000361302.3:p.Val465=
ENST00000402686.7:c.1328T= ENSP00000385797.3:p.Val443=
ENST00000404875.6:c.977T= ENSP00000384531.2:p.Val326=
ENST00000423007.5:c.1328T= ENSP00000404119.1:p.Val443=
ENST00000485278.5:n.1883T=
NM_001077365.1:c.1328T= NP_001070833.1:p.Val443=
NM_001077366.1:c.1166T= NP_001070834.1:p.Val389=
NM_001136113.1:c.1328T= NP_001129585.1:p.Val443=
NM_001136114.1:c.977T= NP_001129586.1:p.Val326=
NM_007171.3:c.1394T= NP_009102.3:p.Val465=
XM_005272156.1:c.1394T= XP_005272213.1:p.Val465=
XM_005272158.1:c.1232T= XP_005272215.1:p.Val411=
XM_005272159.1:c.1043T= XP_005272216.1:p.Val348=
XM_005272162.1:c.197T= XP_005272219.1:p.Val66=
XM_006716932.1:c.1043T= XP_006716995.1:p.Val348=
XM_011518140.1:c.1247T= XP_011516442.1:p.Val416=
XM_011518141.1:c.1181T= XP_011516443.1:p.Val394=
XM_011518142.1:c.1085T= XP_011516444.1:p.Val362=
XM_011518143.1:c.1079T= XP_011516445.1:p.Val360=
XM_011518144.1:c.1394T= XP_011516446.1:p.Val465=
XM_011518145.1:c.938T= XP_011516447.1:p.Val313=
XM_011518146.1:c.1079T= XP_011516448.1:p.Val360=
XM_011518147.1:c.266T= XP_011516449.1:p.Val89=
XR_929703.1:n.1570T=
NM_001353193.1:c.1394T= NP_001340122.1:p.Val465=
NM_001353194.1:c.1166T= NP_001340123.1:p.Val389=
NM_001353195.1:c.977T= NP_001340124.1:p.Val326=
NM_001353196.1:c.1238T= NP_001340125.1:p.Val413=
NM_001353197.1:c.1232T= NP_001340126.1:p.Val411=
NM_001353198.1:c.1232T= NP_001340127.1:p.Val411=
NM_001353199.1:c.1043T= NP_001340128.1:p.Val348=
NM_001353200.1:c.872T= NP_001340129.1:p.Val291=
NR_148391.1:n.1378T=
NR_148392.1:n.1596T=
NR_148393.1:n.1378T=
NR_148394.1:n.1271T=
NR_148395.1:n.1530T=
NR_148396.1:n.1164T=
NR_148397.1:n.1428T=
NR_148398.1:n.1383T=
NR_148399.1:n.1770T=
NR_148400.1:n.1369T=
XM_005272162.3:c.197T= XP_005272219.1:p.Val66=
XM_006716932.2:c.1043T= XP_006716995.1:p.Val348=
XM_011518140.2:c.1247T= XP_011516442.1:p.Val416=
XM_011518141.2:c.1181T= XP_011516443.1:p.Val394=
XM_011518142.2:c.1085T= XP_011516444.1:p.Val362=
XM_011518143.2:c.1079T= XP_011516445.1:p.Val360=
XM_011518145.2:c.938T= XP_011516447.1:p.Val313=
XM_017014205.2:c.197T= XP_016869694.1:p.Val66=
XM_024447380.1:c.197T= XP_024303148.1:p.Val66=
XM_024447381.1:c.503T= XP_024303149.1:p.Val168=
XM_024447382.1:c.197T= XP_024303150.1:p.Val66=
XR_001746160.2:n.1498T=
XR_001746162.2:n.1564T=
XR_001746164.1:n.1281T=
XR_001746166.2:n.1715T=
NM_001077365.2:c.1328T= MANE Select NP_001070833.1:p.Val443=
NM_001077366.2:c.1166T= NP_001070834.1:p.Val389=
NM_001136113.2:c.1328T= NP_001129585.1:p.Val443=
NM_001136114.2:c.977T= NP_001129586.1:p.Val326=
NM_001353193.2:c.1394T= NP_001340122.2:p.Val465=
NM_001353194.2:c.1166T= NP_001340123.1:p.Val389=
NM_001353195.2:c.977T= NP_001340124.1:p.Val326=
NM_001353196.2:c.1238T= NP_001340125.1:p.Val413=
NM_001353197.2:c.1232T= NP_001340126.2:p.Val411=
NM_001353198.2:c.1232T= NP_001340127.2:p.Val411=
NM_001353199.2:c.1043T= NP_001340128.2:p.Val348=
NM_001353200.2:c.872T= NP_001340129.1:p.Val291=
NM_001374689.1:c.1316T= NP_001361618.1:p.Val439=
NM_001374690.1:c.1328T= NP_001361619.1:p.Val443=
NM_001374691.1:c.977T= NP_001361620.1:p.Val326=
NM_001374692.1:c.977T= NP_001361621.1:p.Val326=
NM_001374693.1:c.977T= NP_001361622.1:p.Val326=
NM_001374695.1:c.938T= NP_001361624.1:p.Val313=
NM_007171.4:c.1394T= NP_009102.4:p.Val465=
NR_148391.2:n.1362T=
NR_148392.2:n.1580T=
NR_148393.2:n.1362T=
NR_148394.2:n.1255T=
NR_148395.2:n.1514T=
NR_148396.2:n.1148T=
NR_148397.2:n.1412T=
NR_148398.2:n.1367T=
NR_148399.2:n.1754T=
NR_148400.2:n.1353T=