Canonical Allele Identifier: CA1881751889
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131518503G= , CM000671.2:g.131518503G= GRCh38
NC_000009.11:g.134393890G= , CM000671.1:g.134393890G= GRCh37
NC_000009.10:g.133383711G= NCBI36
NG_008896.1:g.20602G=
NG_008896.2:g.20602G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1169G= ENSP00000343034.7:p.Arg390=
ENST00000404875.7:n.1871G=
ENST00000423007.6:c.1388G= ENSP00000404119.2:p.Arg463=
ENST00000677295.2:c.*1675G= ENSP00000504346.2:n.*1675G=
ENST00000678264.2:c.*1514G= ENSP00000503157.2:n.*1514G=
ENST00000682070.1:n.1796G=
ENST00000682535.1:n.103G=
ENST00000682539.1:c.269G=
ENST00000682813.1:n.1596G=
ENST00000683110.1:n.59G=
ENST00000683392.1:n.4078G=
ENST00000683712.1:n.1736G=
ENST00000683900.1:n.3231G=
ENST00000684062.1:n.1997G=
ENST00000684579.1:n.3177G=
ENST00000684679.1:n.558G=
ENST00000341012.12:c.1169G= ENSP00000343034.7:p.Arg390=
ENST00000372220.5:c.200G= ENSP00000361294.5:p.Arg67=
ENST00000372228.9:c.1397G= ENSP00000361302.3:p.Arg466=
ENST00000402686.8:c.1331G= MANE Select ENSP00000385797.4:p.Arg444=
ENST00000676640.1:c.1331G= ENSP00000503281.1:p.Arg444=
ENST00000676803.1:c.506G= ENSP00000503093.1:p.Arg169=
ENST00000676835.1:c.*546G= ENSP00000502911.1:n.*546G=
ENST00000677029.1:c.875G= ENSP00000502936.1:p.Arg292=
ENST00000677099.1:c.*1041G= ENSP00000504553.1:n.*1041G=
ENST00000677216.1:c.980G= ENSP00000503772.1:p.Arg327=
ENST00000677221.1:n.356G=
ENST00000677295.1:c.*708G= ENSP00000504346.1:n.*708G=
ENST00000677444.1:c.1137G=
ENST00000677586.1:n.812G=
ENST00000677626.1:c.980G= ENSP00000503552.1:p.Arg327=
ENST00000677677.1:n.1291G=
ENST00000677853.1:c.*339G= ENSP00000503488.1:n.*339G=
ENST00000677983.1:n.420G=
ENST00000678202.1:n.351G=
ENST00000678264.1:c.*708G= ENSP00000503157.1:n.*708G=
ENST00000678303.1:c.1241G= ENSP00000503696.1:p.Arg414=
ENST00000678366.1:c.*1580G= ENSP00000504353.1:n.*1580G=
ENST00000678546.1:c.*1276G= ENSP00000503062.1:n.*1276G=
ENST00000678548.1:c.*1403G= ENSP00000503934.1:n.*1403G=
ENST00000678626.1:n.1028G=
ENST00000678733.1:c.412G=
ENST00000678739.1:c.*1657G= ENSP00000503806.1:n.*1657G=
ENST00000678795.1:n.418G=
ENST00000678833.1:c.*778G= ENSP00000503893.1:n.*778G=
ENST00000678942.1:c.511G= ENSP00000504690.1:n.511G=
ENST00000679023.1:c.1169G= ENSP00000503718.1:p.Arg390=
ENST00000679076.1:c.950G=
ENST00000679111.1:c.1331G= ENSP00000504257.1:p.Arg444=
ENST00000679189.1:c.980G= ENSP00000503356.1:p.Arg327=
ENST00000341012.11:c.1169G= ENSP00000343034.7:p.Arg390=
ENST00000372220.4:c.194G= ENSP00000361294.4:p.Arg65=
ENST00000372228.7:c.1397G= ENSP00000361302.3:p.Arg466=
ENST00000402686.7:c.1331G= ENSP00000385797.3:p.Arg444=
ENST00000404875.6:c.980G= ENSP00000384531.2:p.Arg327=
ENST00000423007.5:c.1331G= ENSP00000404119.1:p.Arg444=
ENST00000485278.5:n.1886G=
NM_001077365.1:c.1331G= NP_001070833.1:p.Arg444=
NM_001077366.1:c.1169G= NP_001070834.1:p.Arg390=
NM_001136113.1:c.1331G= NP_001129585.1:p.Arg444=
NM_001136114.1:c.980G= NP_001129586.1:p.Arg327=
NM_007171.3:c.1397G= NP_009102.3:p.Arg466=
XM_005272156.1:c.1397G= XP_005272213.1:p.Arg466=
XM_005272158.1:c.1235G= XP_005272215.1:p.Arg412=
XM_005272159.1:c.1046G= XP_005272216.1:p.Arg349=
XM_005272162.1:c.200G= XP_005272219.1:p.Arg67=
XM_006716932.1:c.1046G= XP_006716995.1:p.Arg349=
XM_011518140.1:c.1250G= XP_011516442.1:p.Arg417=
XM_011518141.1:c.1184G= XP_011516443.1:p.Arg395=
XM_011518142.1:c.1088G= XP_011516444.1:p.Arg363=
XM_011518143.1:c.1082G= XP_011516445.1:p.Arg361=
XM_011518144.1:c.1397G= XP_011516446.1:p.Arg466=
XM_011518145.1:c.941G= XP_011516447.1:p.Arg314=
XM_011518146.1:c.1082G= XP_011516448.1:p.Arg361=
XM_011518147.1:c.269G= XP_011516449.1:p.Arg90=
XR_929703.1:n.1573G=
NM_001353193.1:c.1397G= NP_001340122.1:p.Arg466=
NM_001353194.1:c.1169G= NP_001340123.1:p.Arg390=
NM_001353195.1:c.980G= NP_001340124.1:p.Arg327=
NM_001353196.1:c.1241G= NP_001340125.1:p.Arg414=
NM_001353197.1:c.1235G= NP_001340126.1:p.Arg412=
NM_001353198.1:c.1235G= NP_001340127.1:p.Arg412=
NM_001353199.1:c.1046G= NP_001340128.1:p.Arg349=
NM_001353200.1:c.875G= NP_001340129.1:p.Arg292=
NR_148391.1:n.1381G=
NR_148392.1:n.1599G=
NR_148393.1:n.1381G=
NR_148394.1:n.1274G=
NR_148395.1:n.1533G=
NR_148396.1:n.1167G=
NR_148397.1:n.1431G=
NR_148398.1:n.1386G=
NR_148399.1:n.1773G=
NR_148400.1:n.1372G=
XM_005272162.3:c.200G= XP_005272219.1:p.Arg67=
XM_006716932.2:c.1046G= XP_006716995.1:p.Arg349=
XM_011518140.2:c.1250G= XP_011516442.1:p.Arg417=
XM_011518141.2:c.1184G= XP_011516443.1:p.Arg395=
XM_011518142.2:c.1088G= XP_011516444.1:p.Arg363=
XM_011518143.2:c.1082G= XP_011516445.1:p.Arg361=
XM_011518145.2:c.941G= XP_011516447.1:p.Arg314=
XM_017014205.2:c.200G= XP_016869694.1:p.Arg67=
XM_024447380.1:c.200G= XP_024303148.1:p.Arg67=
XM_024447381.1:c.506G= XP_024303149.1:p.Arg169=
XM_024447382.1:c.200G= XP_024303150.1:p.Arg67=
XR_001746160.2:n.1501G=
XR_001746162.2:n.1567G=
XR_001746164.1:n.1284G=
XR_001746166.2:n.1718G=
NM_001077365.2:c.1331G= MANE Select NP_001070833.1:p.Arg444=
NM_001077366.2:c.1169G= NP_001070834.1:p.Arg390=
NM_001136113.2:c.1331G= NP_001129585.1:p.Arg444=
NM_001136114.2:c.980G= NP_001129586.1:p.Arg327=
NM_001353193.2:c.1397G= NP_001340122.2:p.Arg466=
NM_001353194.2:c.1169G= NP_001340123.1:p.Arg390=
NM_001353195.2:c.980G= NP_001340124.1:p.Arg327=
NM_001353196.2:c.1241G= NP_001340125.1:p.Arg414=
NM_001353197.2:c.1235G= NP_001340126.2:p.Arg412=
NM_001353198.2:c.1235G= NP_001340127.2:p.Arg412=
NM_001353199.2:c.1046G= NP_001340128.2:p.Arg349=
NM_001353200.2:c.875G= NP_001340129.1:p.Arg292=
NM_001374689.1:c.1319G= NP_001361618.1:p.Arg440=
NM_001374690.1:c.1331G= NP_001361619.1:p.Arg444=
NM_001374691.1:c.980G= NP_001361620.1:p.Arg327=
NM_001374692.1:c.980G= NP_001361621.1:p.Arg327=
NM_001374693.1:c.980G= NP_001361622.1:p.Arg327=
NM_001374695.1:c.941G= NP_001361624.1:p.Arg314=
NM_007171.4:c.1397G= NP_009102.4:p.Arg466=
NR_148391.2:n.1365G=
NR_148392.2:n.1583G=
NR_148393.2:n.1365G=
NR_148394.2:n.1258G=
NR_148395.2:n.1517G=
NR_148396.2:n.1151G=
NR_148397.2:n.1415G=
NR_148398.2:n.1370G=
NR_148399.2:n.1757G=
NR_148400.2:n.1356G=