Canonical Allele Identifier: CA1881751810
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518465T= , CM000671.2:g.131518465T= GRCh38
NC_000009.11:g.134393852T= , CM000671.1:g.134393852T= GRCh37
NC_000009.10:g.133383673T= NCBI36
NG_008896.1:g.20564T=
NG_008896.2:g.20564T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1131T= ENSP00000343034.7:p.Ser377=
ENST00000404875.7:n.1833T=
ENST00000423007.6:c.1350T= ENSP00000404119.2:p.Ser450=
ENST00000677295.2:c.*1637T= ENSP00000504346.2:n.*1637T=
ENST00000678264.2:c.*1476T= ENSP00000503157.2:n.*1476T=
ENST00000682070.1:n.1758T=
ENST00000682535.1:n.65T=
ENST00000682539.1:c.231T=
ENST00000682813.1:n.1558T=
ENST00000683110.1:n.21T=
ENST00000683392.1:n.4040T=
ENST00000683712.1:n.1698T=
ENST00000683900.1:n.3193T=
ENST00000684062.1:n.1959T=
ENST00000684579.1:n.3139T=
ENST00000684679.1:n.520T=
ENST00000341012.12:c.1131T= ENSP00000343034.7:p.Ser377=
ENST00000372220.5:c.162T= ENSP00000361294.5:p.Ser54=
ENST00000372228.9:c.1359T= ENSP00000361302.3:p.Ser453=
ENST00000402686.8:c.1293T= MANE Select ENSP00000385797.4:p.Ser431=
ENST00000676640.1:c.1293T= ENSP00000503281.1:p.Ser431=
ENST00000676803.1:c.468T= ENSP00000503093.1:p.Ser156=
ENST00000676835.1:c.*508T= ENSP00000502911.1:n.*508T=
ENST00000677029.1:c.837T= ENSP00000502936.1:p.Ser279=
ENST00000677099.1:c.*1003T= ENSP00000504553.1:n.*1003T=
ENST00000677216.1:c.942T= ENSP00000503772.1:p.Ser314=
ENST00000677221.1:n.318T=
ENST00000677295.1:c.*670T= ENSP00000504346.1:n.*670T=
ENST00000677444.1:c.1099T=
ENST00000677586.1:n.774T=
ENST00000677626.1:c.942T= ENSP00000503552.1:p.Ser314=
ENST00000677677.1:n.1253T=
ENST00000677853.1:c.*301T= ENSP00000503488.1:n.*301T=
ENST00000677983.1:n.382T=
ENST00000678202.1:n.313T=
ENST00000678264.1:c.*670T= ENSP00000503157.1:n.*670T=
ENST00000678303.1:c.1203T= ENSP00000503696.1:p.Ser401=
ENST00000678366.1:c.*1542T= ENSP00000504353.1:n.*1542T=
ENST00000678546.1:c.*1238T= ENSP00000503062.1:n.*1238T=
ENST00000678548.1:c.*1365T= ENSP00000503934.1:n.*1365T=
ENST00000678626.1:n.990T=
ENST00000678733.1:c.374T=
ENST00000678739.1:c.*1619T= ENSP00000503806.1:n.*1619T=
ENST00000678795.1:n.380T=
ENST00000678833.1:c.*740T= ENSP00000503893.1:n.*740T=
ENST00000678942.1:c.473T= ENSP00000504690.1:n.473T=
ENST00000679023.1:c.1131T= ENSP00000503718.1:p.Ser377=
ENST00000679076.1:c.912T=
ENST00000679111.1:c.1293T= ENSP00000504257.1:p.Ser431=
ENST00000679189.1:c.942T= ENSP00000503356.1:p.Ser314=
ENST00000341012.11:c.1131T= ENSP00000343034.7:p.Ser377=
ENST00000372220.4:c.156T= ENSP00000361294.4:p.Ser52=
ENST00000372228.7:c.1359T= ENSP00000361302.3:p.Ser453=
ENST00000402686.7:c.1293T= ENSP00000385797.3:p.Ser431=
ENST00000404875.6:c.942T= ENSP00000384531.2:p.Ser314=
ENST00000423007.5:c.1293T= ENSP00000404119.1:p.Ser431=
ENST00000485278.5:n.1848T=
NM_001077365.1:c.1293T= NP_001070833.1:p.Ser431=
NM_001077366.1:c.1131T= NP_001070834.1:p.Ser377=
NM_001136113.1:c.1293T= NP_001129585.1:p.Ser431=
NM_001136114.1:c.942T= NP_001129586.1:p.Ser314=
NM_007171.3:c.1359T= NP_009102.3:p.Ser453=
XM_005272156.1:c.1359T= XP_005272213.1:p.Ser453=
XM_005272158.1:c.1197T= XP_005272215.1:p.Ser399=
XM_005272159.1:c.1008T= XP_005272216.1:p.Ser336=
XM_005272162.1:c.162T= XP_005272219.1:p.Ser54=
XM_006716932.1:c.1008T= XP_006716995.1:p.Ser336=
XM_011518140.1:c.1212T= XP_011516442.1:p.Ser404=
XM_011518141.1:c.1146T= XP_011516443.1:p.Ser382=
XM_011518142.1:c.1050T= XP_011516444.1:p.Ser350=
XM_011518143.1:c.1044T= XP_011516445.1:p.Ser348=
XM_011518144.1:c.1359T= XP_011516446.1:p.Ser453=
XM_011518145.1:c.903T= XP_011516447.1:p.Ser301=
XM_011518146.1:c.1044T= XP_011516448.1:p.Ser348=
XM_011518147.1:c.231T= XP_011516449.1:p.Ser77=
XR_929703.1:n.1535T=
NM_001353193.1:c.1359T= NP_001340122.1:p.Ser453=
NM_001353194.1:c.1131T= NP_001340123.1:p.Ser377=
NM_001353195.1:c.942T= NP_001340124.1:p.Ser314=
NM_001353196.1:c.1203T= NP_001340125.1:p.Ser401=
NM_001353197.1:c.1197T= NP_001340126.1:p.Ser399=
NM_001353198.1:c.1197T= NP_001340127.1:p.Ser399=
NM_001353199.1:c.1008T= NP_001340128.1:p.Ser336=
NM_001353200.1:c.837T= NP_001340129.1:p.Ser279=
NR_148391.1:n.1343T=
NR_148392.1:n.1561T=
NR_148393.1:n.1343T=
NR_148394.1:n.1236T=
NR_148395.1:n.1495T=
NR_148396.1:n.1129T=
NR_148397.1:n.1393T=
NR_148398.1:n.1348T=
NR_148399.1:n.1735T=
NR_148400.1:n.1334T=
XM_005272162.3:c.162T= XP_005272219.1:p.Ser54=
XM_006716932.2:c.1008T= XP_006716995.1:p.Ser336=
XM_011518140.2:c.1212T= XP_011516442.1:p.Ser404=
XM_011518141.2:c.1146T= XP_011516443.1:p.Ser382=
XM_011518142.2:c.1050T= XP_011516444.1:p.Ser350=
XM_011518143.2:c.1044T= XP_011516445.1:p.Ser348=
XM_011518145.2:c.903T= XP_011516447.1:p.Ser301=
XM_017014205.2:c.162T= XP_016869694.1:p.Ser54=
XM_024447380.1:c.162T= XP_024303148.1:p.Ser54=
XM_024447381.1:c.468T= XP_024303149.1:p.Ser156=
XM_024447382.1:c.162T= XP_024303150.1:p.Ser54=
XR_001746160.2:n.1463T=
XR_001746162.2:n.1529T=
XR_001746164.1:n.1246T=
XR_001746166.2:n.1680T=
NM_001077365.2:c.1293T= MANE Select NP_001070833.1:p.Ser431=
NM_001077366.2:c.1131T= NP_001070834.1:p.Ser377=
NM_001136113.2:c.1293T= NP_001129585.1:p.Ser431=
NM_001136114.2:c.942T= NP_001129586.1:p.Ser314=
NM_001353193.2:c.1359T= NP_001340122.2:p.Ser453=
NM_001353194.2:c.1131T= NP_001340123.1:p.Ser377=
NM_001353195.2:c.942T= NP_001340124.1:p.Ser314=
NM_001353196.2:c.1203T= NP_001340125.1:p.Ser401=
NM_001353197.2:c.1197T= NP_001340126.2:p.Ser399=
NM_001353198.2:c.1197T= NP_001340127.2:p.Ser399=
NM_001353199.2:c.1008T= NP_001340128.2:p.Ser336=
NM_001353200.2:c.837T= NP_001340129.1:p.Ser279=
NM_001374689.1:c.1281T= NP_001361618.1:p.Ser427=
NM_001374690.1:c.1293T= NP_001361619.1:p.Ser431=
NM_001374691.1:c.942T= NP_001361620.1:p.Ser314=
NM_001374692.1:c.942T= NP_001361621.1:p.Ser314=
NM_001374693.1:c.942T= NP_001361622.1:p.Ser314=
NM_001374695.1:c.903T= NP_001361624.1:p.Ser301=
NM_007171.4:c.1359T= NP_009102.4:p.Ser453=
NR_148391.2:n.1327T=
NR_148392.2:n.1545T=
NR_148393.2:n.1327T=
NR_148394.2:n.1220T=
NR_148395.2:n.1479T=
NR_148396.2:n.1113T=
NR_148397.2:n.1377T=
NR_148398.2:n.1332T=
NR_148399.2:n.1719T=
NR_148400.2:n.1318T=