Canonical Allele Identifier: CA1881752737
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518928G= , CM000671.2:g.131518928G= GRCh38
NC_000009.11:g.134394315G= , CM000671.1:g.134394315G= GRCh37
NC_000009.10:g.133384136G= NCBI36
NG_008896.1:g.21027G=
NG_008896.2:g.21027G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1295G= ENSP00000343034.7:p.Trp432=
ENST00000404875.7:n.1997G=
ENST00000423007.6:c.1514G= ENSP00000404119.2:p.Trp505=
ENST00000677295.2:c.*1801G= ENSP00000504346.2:n.*1801G=
ENST00000678264.2:c.*1640G= ENSP00000503157.2:n.*1640G=
ENST00000682070.1:n.1922G=
ENST00000682539.1:c.395G=
ENST00000682813.1:n.1861G=
ENST00000683392.1:n.4204G=
ENST00000683712.1:n.1862G=
ENST00000683900.1:n.3357G=
ENST00000684062.1:n.2123G=
ENST00000684579.1:n.3303G=
ENST00000684679.1:n.684G=
ENST00000341012.12:c.1295G= ENSP00000343034.7:p.Trp432=
ENST00000372220.5:c.326G= ENSP00000361294.5:p.Trp109=
ENST00000372228.9:c.1523G= ENSP00000361302.3:p.Trp508=
ENST00000402686.8:c.1457G= MANE Select ENSP00000385797.4:p.Trp486=
ENST00000676640.1:c.1457G= ENSP00000503281.1:p.Trp486=
ENST00000676803.1:c.632G= ENSP00000503093.1:p.Trp211=
ENST00000676835.1:c.*672G= ENSP00000502911.1:n.*672G=
ENST00000677029.1:c.1001G= ENSP00000502936.1:p.Trp334=
ENST00000677099.1:c.*1167G= ENSP00000504553.1:n.*1167G=
ENST00000677216.1:c.1106G= ENSP00000503772.1:p.Trp369=
ENST00000677221.1:n.482G=
ENST00000677295.1:c.*834G= ENSP00000504346.1:n.*834G=
ENST00000677444.1:c.1402G=
ENST00000677586.1:n.938G=
ENST00000677626.1:c.1106G= ENSP00000503552.1:p.Trp369=
ENST00000677677.1:n.1417G=
ENST00000677853.1:c.*465G= ENSP00000503488.1:n.*465G=
ENST00000678202.1:n.616G=
ENST00000678264.1:c.*834G= ENSP00000503157.1:n.*834G=
ENST00000678303.1:c.1367G= ENSP00000503696.1:p.Trp456=
ENST00000678366.1:c.*1706G= ENSP00000504353.1:n.*1706G=
ENST00000678546.1:c.*1402G= ENSP00000503062.1:n.*1402G=
ENST00000678548.1:c.*1529G= ENSP00000503934.1:n.*1529G=
ENST00000678626.1:n.1293G=
ENST00000678733.1:c.538G=
ENST00000678739.1:c.*1783G= ENSP00000503806.1:n.*1783G=
ENST00000678833.1:c.*904G= ENSP00000503893.1:n.*904G=
ENST00000679023.1:c.1295G= ENSP00000503718.1:p.Trp432=
ENST00000679076.1:c.1076G=
ENST00000679111.1:c.*213G= ENSP00000504257.1:n.*213G=
ENST00000679189.1:c.1106G= ENSP00000503356.1:p.Trp369=
ENST00000341012.11:c.1295G= ENSP00000343034.7:p.Trp432=
ENST00000372220.4:c.320G= ENSP00000361294.4:p.Trp107=
ENST00000372228.7:c.1523G= ENSP00000361302.3:p.Trp508=
ENST00000402686.7:c.1457G= ENSP00000385797.3:p.Trp486=
ENST00000404875.6:c.1106G= ENSP00000384531.2:p.Trp369=
ENST00000423007.5:c.1457G= ENSP00000404119.1:p.Trp486=
ENST00000467848.1:n.161G=
ENST00000485278.5:n.2012G=
NM_001077365.1:c.1457G= NP_001070833.1:p.Trp486=
NM_001077366.1:c.1295G= NP_001070834.1:p.Trp432=
NM_001136113.1:c.1457G= NP_001129585.1:p.Trp486=
NM_001136114.1:c.1106G= NP_001129586.1:p.Trp369=
NM_007171.3:c.1523G= NP_009102.3:p.Trp508=
XM_005272156.1:c.1523G= XP_005272213.1:p.Trp508=
XM_005272158.1:c.1361G= XP_005272215.1:p.Trp454=
XM_005272159.1:c.1172G= XP_005272216.1:p.Trp391=
XM_005272162.1:c.326G= XP_005272219.1:p.Trp109=
XM_006716932.1:c.1172G= XP_006716995.1:p.Trp391=
XM_011518140.1:c.1376G= XP_011516442.1:p.Trp459=
XM_011518141.1:c.1310G= XP_011516443.1:p.Trp437=
XM_011518142.1:c.1214G= XP_011516444.1:p.Trp405=
XM_011518143.1:c.1208G= XP_011516445.1:p.Trp403=
XM_011518145.1:c.1067G= XP_011516447.1:p.Trp356=
XM_011518147.1:c.395G= XP_011516449.1:p.Trp132=
XR_929703.1:n.1699G=
NM_001353193.1:c.1523G= NP_001340122.1:p.Trp508=
NM_001353194.1:c.1295G= NP_001340123.1:p.Trp432=
NM_001353195.1:c.1106G= NP_001340124.1:p.Trp369=
NM_001353196.1:c.1367G= NP_001340125.1:p.Trp456=
NM_001353197.1:c.1361G= NP_001340126.1:p.Trp454=
NM_001353198.1:c.1361G= NP_001340127.1:p.Trp454=
NM_001353199.1:c.1172G= NP_001340128.1:p.Trp391=
NM_001353200.1:c.1001G= NP_001340129.1:p.Trp334=
NR_148391.1:n.1507G=
NR_148392.1:n.1725G=
NR_148393.1:n.1646G=
NR_148394.1:n.1400G=
NR_148395.1:n.1798G=
NR_148396.1:n.1432G=
NR_148397.1:n.1557G=
NR_148398.1:n.1512G=
NR_148399.1:n.2038G=
NR_148400.1:n.1637G=
XM_005272162.3:c.326G= XP_005272219.1:p.Trp109=
XM_006716932.2:c.1172G= XP_006716995.1:p.Trp391=
XM_011518140.2:c.1376G= XP_011516442.1:p.Trp459=
XM_011518141.2:c.1310G= XP_011516443.1:p.Trp437=
XM_011518142.2:c.1214G= XP_011516444.1:p.Trp405=
XM_011518143.2:c.1208G= XP_011516445.1:p.Trp403=
XM_011518145.2:c.1067G= XP_011516447.1:p.Trp356=
XM_017014205.2:c.326G= XP_016869694.1:p.Trp109=
XM_024447380.1:c.326G= XP_024303148.1:p.Trp109=
XM_024447381.1:c.632G= XP_024303149.1:p.Trp211=
XM_024447382.1:c.326G= XP_024303150.1:p.Trp109=
XR_001746160.2:n.1627G=
XR_001746162.2:n.1832G=
XR_001746164.1:n.1549G=
XR_001746166.2:n.1844G=
NM_001077365.2:c.1457G= MANE Select NP_001070833.1:p.Trp486=
NM_001077366.2:c.1295G= NP_001070834.1:p.Trp432=
NM_001136113.2:c.1457G= NP_001129585.1:p.Trp486=
NM_001136114.2:c.1106G= NP_001129586.1:p.Trp369=
NM_001353193.2:c.1523G= NP_001340122.2:p.Trp508=
NM_001353194.2:c.1295G= NP_001340123.1:p.Trp432=
NM_001353195.2:c.1106G= NP_001340124.1:p.Trp369=
NM_001353196.2:c.1367G= NP_001340125.1:p.Trp456=
NM_001353197.2:c.1361G= NP_001340126.2:p.Trp454=
NM_001353198.2:c.1361G= NP_001340127.2:p.Trp454=
NM_001353199.2:c.1172G= NP_001340128.2:p.Trp391=
NM_001353200.2:c.1001G= NP_001340129.1:p.Trp334=
NM_001374689.1:c.1445G= NP_001361618.1:p.Trp482=
NM_001374690.1:c.1365+391G= NP_001361619.1:n.1365+391G=
NM_001374691.1:c.1106G= NP_001361620.1:p.Trp369=
NM_001374692.1:c.1106G= NP_001361621.1:p.Trp369=
NM_001374693.1:c.1106G= NP_001361622.1:p.Trp369=
NM_001374695.1:c.1067G= NP_001361624.1:p.Trp356=
NM_007171.4:c.1523G= NP_009102.4:p.Trp508=
NR_148391.2:n.1491G=
NR_148392.2:n.1709G=
NR_148393.2:n.1630G=
NR_148394.2:n.1384G=
NR_148395.2:n.1782G=
NR_148396.2:n.1416G=
NR_148397.2:n.1541G=
NR_148398.2:n.1496G=
NR_148399.2:n.2022G=
NR_148400.2:n.1621G=