Canonical Allele Identifier: CA375312076
Gene: POMT1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518933G>T , CM000671.2:g.131518933G>T GRCh38
NC_000009.11:g.134394320G>T , CM000671.1:g.134394320G>T GRCh37
NC_000009.10:g.133384141G>T NCBI36
NG_008896.1:g.21032G>T
NG_008896.2:g.21032G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1300G>T ENSP00000343034.7:p.Val434Leu
ENST00000404875.7:n.2002G>T
ENST00000423007.6:c.1519G>T ENSP00000404119.2:p.Val507Leu
ENST00000677295.2:c.*1806G>T ENSP00000504346.2:n.*1806G>T
ENST00000678264.2:c.*1645G>T ENSP00000503157.2:n.*1645G>T
ENST00000682070.1:n.1927G>T
ENST00000682539.1:c.400G>T
ENST00000682813.1:n.1866G>T
ENST00000683392.1:n.4209G>T
ENST00000683712.1:n.1867G>T
ENST00000683900.1:n.3362G>T
ENST00000684062.1:n.2128G>T
ENST00000684579.1:n.3308G>T
ENST00000684679.1:n.689G>T
ENST00000341012.12:c.1300G>T ENSP00000343034.7:p.Val434Leu
ENST00000372220.5:c.331G>T ENSP00000361294.5:p.Val111Leu
ENST00000372228.9:c.1528G>T ENSP00000361302.3:p.Val510Leu
ENST00000402686.8:c.1462G>T MANE Select ENSP00000385797.4:p.Val488Leu
ENST00000676640.1:c.1462G>T ENSP00000503281.1:p.Val488Leu
ENST00000676803.1:c.637G>T ENSP00000503093.1:p.Val213Leu
ENST00000676835.1:c.*677G>T ENSP00000502911.1:n.*677G>T
ENST00000677029.1:c.1006G>T ENSP00000502936.1:p.Val336Leu
ENST00000677099.1:c.*1172G>T ENSP00000504553.1:n.*1172G>T
ENST00000677216.1:c.1111G>T ENSP00000503772.1:p.Val371Leu
ENST00000677221.1:n.487G>T
ENST00000677295.1:c.*839G>T ENSP00000504346.1:n.*839G>T
ENST00000677444.1:c.1407G>T
ENST00000677586.1:n.943G>T
ENST00000677626.1:c.1111G>T ENSP00000503552.1:p.Val371Leu
ENST00000677677.1:n.1422G>T
ENST00000677853.1:c.*470G>T ENSP00000503488.1:n.*470G>T
ENST00000678202.1:n.621G>T
ENST00000678264.1:c.*839G>T ENSP00000503157.1:n.*839G>T
ENST00000678303.1:c.1372G>T ENSP00000503696.1:p.Val458Leu
ENST00000678366.1:c.*1711G>T ENSP00000504353.1:n.*1711G>T
ENST00000678546.1:c.*1407G>T ENSP00000503062.1:n.*1407G>T
ENST00000678548.1:c.*1534G>T ENSP00000503934.1:n.*1534G>T
ENST00000678626.1:n.1298G>T
ENST00000678733.1:c.543G>T
ENST00000678739.1:c.*1788G>T ENSP00000503806.1:n.*1788G>T
ENST00000678833.1:c.*909G>T ENSP00000503893.1:n.*909G>T
ENST00000679023.1:c.1300G>T ENSP00000503718.1:p.Val434Leu
ENST00000679076.1:c.1081G>T
ENST00000679111.1:c.*218G>T ENSP00000504257.1:n.*218G>T
ENST00000679189.1:c.1111G>T ENSP00000503356.1:p.Val371Leu
ENST00000341012.11:c.1300G>T ENSP00000343034.7:p.Val434Leu
ENST00000372220.4:c.325G>T ENSP00000361294.4:p.Val109Leu
ENST00000372228.7:c.1528G>T ENSP00000361302.3:p.Val510Leu
ENST00000402686.7:c.1462G>T ENSP00000385797.3:p.Val488Leu
ENST00000404875.6:c.1111G>T ENSP00000384531.2:p.Val371Leu
ENST00000423007.5:c.1462G>T ENSP00000404119.1:p.Val488Leu
ENST00000467848.1:n.166G>T
ENST00000485278.5:n.2017G>T
NM_001077365.1:c.1462G>T NP_001070833.1:p.Val488Leu
NM_001077366.1:c.1300G>T NP_001070834.1:p.Val434Leu
NM_001136113.1:c.1462G>T NP_001129585.1:p.Val488Leu
NM_001136114.1:c.1111G>T NP_001129586.1:p.Val371Leu
NM_007171.3:c.1528G>T NP_009102.3:p.Val510Leu
XM_005272156.1:c.1528G>T XP_005272213.1:p.Val510Leu
XM_005272158.1:c.1366G>T XP_005272215.1:p.Val456Leu
XM_005272159.1:c.1177G>T XP_005272216.1:p.Val393Leu
XM_005272162.1:c.331G>T XP_005272219.1:p.Val111Leu
XM_006716932.1:c.1177G>T XP_006716995.1:p.Val393Leu
XM_011518140.1:c.1381G>T XP_011516442.1:p.Val461Leu
XM_011518141.1:c.1315G>T XP_011516443.1:p.Val439Leu
XM_011518142.1:c.1219G>T XP_011516444.1:p.Val407Leu
XM_011518143.1:c.1213G>T XP_011516445.1:p.Val405Leu
XM_011518145.1:c.1072G>T XP_011516447.1:p.Val358Leu
XM_011518147.1:c.400G>T XP_011516449.1:p.Val134Leu
XR_929703.1:n.1704G>T
NM_001353193.1:c.1528G>T NP_001340122.1:p.Val510Leu
NM_001353194.1:c.1300G>T NP_001340123.1:p.Val434Leu
NM_001353195.1:c.1111G>T NP_001340124.1:p.Val371Leu
NM_001353196.1:c.1372G>T NP_001340125.1:p.Val458Leu
NM_001353197.1:c.1366G>T NP_001340126.1:p.Val456Leu
NM_001353198.1:c.1366G>T NP_001340127.1:p.Val456Leu
NM_001353199.1:c.1177G>T NP_001340128.1:p.Val393Leu
NM_001353200.1:c.1006G>T NP_001340129.1:p.Val336Leu
NR_148391.1:n.1512G>T
NR_148392.1:n.1730G>T
NR_148393.1:n.1651G>T
NR_148394.1:n.1405G>T
NR_148395.1:n.1803G>T
NR_148396.1:n.1437G>T
NR_148397.1:n.1562G>T
NR_148398.1:n.1517G>T
NR_148399.1:n.2043G>T
NR_148400.1:n.1642G>T
XM_005272162.3:c.331G>T XP_005272219.1:p.Val111Leu
XM_006716932.2:c.1177G>T XP_006716995.1:p.Val393Leu
XM_011518140.2:c.1381G>T XP_011516442.1:p.Val461Leu
XM_011518141.2:c.1315G>T XP_011516443.1:p.Val439Leu
XM_011518142.2:c.1219G>T XP_011516444.1:p.Val407Leu
XM_011518143.2:c.1213G>T XP_011516445.1:p.Val405Leu
XM_011518145.2:c.1072G>T XP_011516447.1:p.Val358Leu
XM_017014205.2:c.331G>T XP_016869694.1:p.Val111Leu
XM_024447380.1:c.331G>T XP_024303148.1:p.Val111Leu
XM_024447381.1:c.637G>T XP_024303149.1:p.Val213Leu
XM_024447382.1:c.331G>T XP_024303150.1:p.Val111Leu
XR_001746160.2:n.1632G>T
XR_001746162.2:n.1837G>T
XR_001746164.1:n.1554G>T
XR_001746166.2:n.1849G>T
NM_001077365.2:c.1462G>T MANE Select NP_001070833.1:p.Val488Leu
NM_001077366.2:c.1300G>T NP_001070834.1:p.Val434Leu
NM_001136113.2:c.1462G>T NP_001129585.1:p.Val488Leu
NM_001136114.2:c.1111G>T NP_001129586.1:p.Val371Leu
NM_001353193.2:c.1528G>T NP_001340122.2:p.Val510Leu
NM_001353194.2:c.1300G>T NP_001340123.1:p.Val434Leu
NM_001353195.2:c.1111G>T NP_001340124.1:p.Val371Leu
NM_001353196.2:c.1372G>T NP_001340125.1:p.Val458Leu
NM_001353197.2:c.1366G>T NP_001340126.2:p.Val456Leu
NM_001353198.2:c.1366G>T NP_001340127.2:p.Val456Leu
NM_001353199.2:c.1177G>T NP_001340128.2:p.Val393Leu
NM_001353200.2:c.1006G>T NP_001340129.1:p.Val336Leu
NM_001374689.1:c.1450G>T NP_001361618.1:p.Val484Leu
NM_001374690.1:c.1365+396G>T NP_001361619.1:n.1365+396G>T
NM_001374691.1:c.1111G>T NP_001361620.1:p.Val371Leu
NM_001374692.1:c.1111G>T NP_001361621.1:p.Val371Leu
NM_001374693.1:c.1111G>T NP_001361622.1:p.Val371Leu
NM_001374695.1:c.1072G>T NP_001361624.1:p.Val358Leu
NM_007171.4:c.1528G>T NP_009102.4:p.Val510Leu
NR_148391.2:n.1496G>T
NR_148392.2:n.1714G>T
NR_148393.2:n.1635G>T
NR_148394.2:n.1389G>T
NR_148395.2:n.1787G>T
NR_148396.2:n.1421G>T
NR_148397.2:n.1546G>T
NR_148398.2:n.1501G>T
NR_148399.2:n.2027G>T
NR_148400.2:n.1626G>T