Canonical Allele Identifier: CA1881752536
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518863G= , CM000671.2:g.131518863G= GRCh38
NC_000009.11:g.134394250G= , CM000671.1:g.134394250G= GRCh37
NC_000009.10:g.133384071G= NCBI36
NG_008896.1:g.20962G=
NG_008896.2:g.20962G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1230G= ENSP00000343034.7:p.Trp410=
ENST00000404875.7:n.1932G=
ENST00000423007.6:c.1449G= ENSP00000404119.2:p.Trp483=
ENST00000677295.2:c.*1736G= ENSP00000504346.2:n.*1736G=
ENST00000678264.2:c.*1575G= ENSP00000503157.2:n.*1575G=
ENST00000682070.1:n.1857G=
ENST00000682539.1:c.330G=
ENST00000682813.1:n.1796G=
ENST00000683392.1:n.4139G=
ENST00000683712.1:n.1797G=
ENST00000683900.1:n.3292G=
ENST00000684062.1:n.2058G=
ENST00000684579.1:n.3238G=
ENST00000684679.1:n.619G=
ENST00000341012.12:c.1230G= ENSP00000343034.7:p.Trp410=
ENST00000372220.5:c.261G= ENSP00000361294.5:p.Trp87=
ENST00000372228.9:c.1458G= ENSP00000361302.3:p.Trp486=
ENST00000402686.8:c.1392G= MANE Select ENSP00000385797.4:p.Trp464=
ENST00000676640.1:c.1392G= ENSP00000503281.1:p.Trp464=
ENST00000676803.1:c.567G= ENSP00000503093.1:p.Trp189=
ENST00000676835.1:c.*607G= ENSP00000502911.1:n.*607G=
ENST00000677029.1:c.936G= ENSP00000502936.1:p.Trp312=
ENST00000677099.1:c.*1102G= ENSP00000504553.1:n.*1102G=
ENST00000677216.1:c.1041G= ENSP00000503772.1:p.Trp347=
ENST00000677221.1:n.417G=
ENST00000677295.1:c.*769G= ENSP00000504346.1:n.*769G=
ENST00000677444.1:c.1337G=
ENST00000677586.1:n.873G=
ENST00000677626.1:c.1041G= ENSP00000503552.1:p.Trp347=
ENST00000677677.1:n.1352G=
ENST00000677853.1:c.*400G= ENSP00000503488.1:n.*400G=
ENST00000678202.1:n.551G=
ENST00000678264.1:c.*769G= ENSP00000503157.1:n.*769G=
ENST00000678303.1:c.1302G= ENSP00000503696.1:p.Trp434=
ENST00000678366.1:c.*1641G= ENSP00000504353.1:n.*1641G=
ENST00000678546.1:c.*1337G= ENSP00000503062.1:n.*1337G=
ENST00000678548.1:c.*1464G= ENSP00000503934.1:n.*1464G=
ENST00000678626.1:n.1228G=
ENST00000678733.1:c.473G=
ENST00000678739.1:c.*1718G= ENSP00000503806.1:n.*1718G=
ENST00000678833.1:c.*839G= ENSP00000503893.1:n.*839G=
ENST00000679023.1:c.1230G= ENSP00000503718.1:p.Trp410=
ENST00000679076.1:c.1011G=
ENST00000679111.1:c.*148G= ENSP00000504257.1:n.*148G=
ENST00000679189.1:c.1041G= ENSP00000503356.1:p.Trp347=
ENST00000341012.11:c.1230G= ENSP00000343034.7:p.Trp410=
ENST00000372220.4:c.255G= ENSP00000361294.4:p.Trp85=
ENST00000372228.7:c.1458G= ENSP00000361302.3:p.Trp486=
ENST00000402686.7:c.1392G= ENSP00000385797.3:p.Trp464=
ENST00000404875.6:c.1041G= ENSP00000384531.2:p.Trp347=
ENST00000423007.5:c.1392G= ENSP00000404119.1:p.Trp464=
ENST00000467848.1:n.96G=
ENST00000485278.5:n.1947G=
NM_001077365.1:c.1392G= NP_001070833.1:p.Trp464=
NM_001077366.1:c.1230G= NP_001070834.1:p.Trp410=
NM_001136113.1:c.1392G= NP_001129585.1:p.Trp464=
NM_001136114.1:c.1041G= NP_001129586.1:p.Trp347=
NM_007171.3:c.1458G= NP_009102.3:p.Trp486=
XM_005272156.1:c.1458G= XP_005272213.1:p.Trp486=
XM_005272158.1:c.1296G= XP_005272215.1:p.Trp432=
XM_005272159.1:c.1107G= XP_005272216.1:p.Trp369=
XM_005272162.1:c.261G= XP_005272219.1:p.Trp87=
XM_006716932.1:c.1107G= XP_006716995.1:p.Trp369=
XM_011518140.1:c.1311G= XP_011516442.1:p.Trp437=
XM_011518141.1:c.1245G= XP_011516443.1:p.Trp415=
XM_011518142.1:c.1149G= XP_011516444.1:p.Trp383=
XM_011518143.1:c.1143G= XP_011516445.1:p.Trp381=
XM_011518144.1:c.*148G= XP_011516446.1:n.*148G=
XM_011518145.1:c.1002G= XP_011516447.1:p.Trp334=
XM_011518146.1:c.*148G= XP_011516448.1:n.*148G=
XM_011518147.1:c.330G= XP_011516449.1:p.Trp110=
XR_929703.1:n.1634G=
NM_001353193.1:c.1458G= NP_001340122.1:p.Trp486=
NM_001353194.1:c.1230G= NP_001340123.1:p.Trp410=
NM_001353195.1:c.1041G= NP_001340124.1:p.Trp347=
NM_001353196.1:c.1302G= NP_001340125.1:p.Trp434=
NM_001353197.1:c.1296G= NP_001340126.1:p.Trp432=
NM_001353198.1:c.1296G= NP_001340127.1:p.Trp432=
NM_001353199.1:c.1107G= NP_001340128.1:p.Trp369=
NM_001353200.1:c.936G= NP_001340129.1:p.Trp312=
NR_148391.1:n.1442G=
NR_148392.1:n.1660G=
NR_148393.1:n.1581G=
NR_148394.1:n.1335G=
NR_148395.1:n.1733G=
NR_148396.1:n.1367G=
NR_148397.1:n.1492G=
NR_148398.1:n.1447G=
NR_148399.1:n.1973G=
NR_148400.1:n.1572G=
XM_005272162.3:c.261G= XP_005272219.1:p.Trp87=
XM_006716932.2:c.1107G= XP_006716995.1:p.Trp369=
XM_011518140.2:c.1311G= XP_011516442.1:p.Trp437=
XM_011518141.2:c.1245G= XP_011516443.1:p.Trp415=
XM_011518142.2:c.1149G= XP_011516444.1:p.Trp383=
XM_011518143.2:c.1143G= XP_011516445.1:p.Trp381=
XM_011518145.2:c.1002G= XP_011516447.1:p.Trp334=
XM_017014205.2:c.261G= XP_016869694.1:p.Trp87=
XM_024447380.1:c.261G= XP_024303148.1:p.Trp87=
XM_024447381.1:c.567G= XP_024303149.1:p.Trp189=
XM_024447382.1:c.261G= XP_024303150.1:p.Trp87=
XR_001746160.2:n.1562G=
XR_001746162.2:n.1767G=
XR_001746164.1:n.1484G=
XR_001746166.2:n.1779G=
NM_001077365.2:c.1392G= MANE Select NP_001070833.1:p.Trp464=
NM_001077366.2:c.1230G= NP_001070834.1:p.Trp410=
NM_001136113.2:c.1392G= NP_001129585.1:p.Trp464=
NM_001136114.2:c.1041G= NP_001129586.1:p.Trp347=
NM_001353193.2:c.1458G= NP_001340122.2:p.Trp486=
NM_001353194.2:c.1230G= NP_001340123.1:p.Trp410=
NM_001353195.2:c.1041G= NP_001340124.1:p.Trp347=
NM_001353196.2:c.1302G= NP_001340125.1:p.Trp434=
NM_001353197.2:c.1296G= NP_001340126.2:p.Trp432=
NM_001353198.2:c.1296G= NP_001340127.2:p.Trp432=
NM_001353199.2:c.1107G= NP_001340128.2:p.Trp369=
NM_001353200.2:c.936G= NP_001340129.1:p.Trp312=
NM_001374689.1:c.1380G= NP_001361618.1:p.Trp460=
NM_001374690.1:c.1365+326G= NP_001361619.1:n.1365+326G=
NM_001374691.1:c.1041G= NP_001361620.1:p.Trp347=
NM_001374692.1:c.1041G= NP_001361621.1:p.Trp347=
NM_001374693.1:c.1041G= NP_001361622.1:p.Trp347=
NM_001374695.1:c.1002G= NP_001361624.1:p.Trp334=
NM_007171.4:c.1458G= NP_009102.4:p.Trp486=
NR_148391.2:n.1426G=
NR_148392.2:n.1644G=
NR_148393.2:n.1565G=
NR_148394.2:n.1319G=
NR_148395.2:n.1717G=
NR_148396.2:n.1351G=
NR_148397.2:n.1476G=
NR_148398.2:n.1431G=
NR_148399.2:n.1957G=
NR_148400.2:n.1556G=