Canonical Allele Identifier: CA1881760361
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523031C= , CM000671.2:g.131523031C= GRCh38
NC_000009.11:g.134398418C= , CM000671.1:g.134398418C= GRCh37
NC_000009.10:g.133388239C= NCBI36
NG_008896.1:g.25130C=
NG_008896.2:g.25130C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1941C= ENSP00000343034.7:p.Asp647=
ENST00000404875.7:n.2643C=
ENST00000423007.6:c.2160C= ENSP00000404119.2:p.Asp720=
ENST00000677295.2:c.*2447C= ENSP00000504346.2:n.*2447C=
ENST00000678264.2:c.*2286C= ENSP00000503157.2:n.*2286C=
ENST00000682070.1:n.2413C=
ENST00000682639.1:c.100C=
ENST00000682813.1:n.2500C=
ENST00000683231.1:c.100C=
ENST00000683392.1:n.4695C=
ENST00000683712.1:n.2508C=
ENST00000683900.1:n.4003C=
ENST00000684062.1:n.2769C=
ENST00000684399.1:c.100C=
ENST00000684579.1:n.3949C=
ENST00000341012.12:c.1941C= ENSP00000343034.7:p.Asp647=
ENST00000372220.5:c.972C= ENSP00000361294.5:p.Asp324=
ENST00000372228.9:c.2169C= ENSP00000361302.3:p.Asp723=
ENST00000402686.8:c.2103C= MANE Select ENSP00000385797.4:p.Asp701=
ENST00000676640.1:c.2103C= ENSP00000503281.1:p.Asp701=
ENST00000676803.1:c.1164C= ENSP00000503093.1:p.Asp388=
ENST00000676835.1:c.*1318C= ENSP00000502911.1:n.*1318C=
ENST00000677029.1:c.1647C= ENSP00000502936.1:p.Asp549=
ENST00000677099.1:c.*1813C= ENSP00000504553.1:n.*1813C=
ENST00000677216.1:c.1752C= ENSP00000503772.1:p.Asp584=
ENST00000677295.1:c.*1325C= ENSP00000504346.1:n.*1325C=
ENST00000677444.1:c.2048C=
ENST00000677586.1:n.1470C=
ENST00000677626.1:c.1752C= ENSP00000503552.1:p.Asp584=
ENST00000677853.1:c.*1111C= ENSP00000503488.1:n.*1111C=
ENST00000678264.1:c.*1480C= ENSP00000503157.1:n.*1480C=
ENST00000678303.1:c.2013C= ENSP00000503696.1:p.Asp671=
ENST00000678366.1:c.*2352C= ENSP00000504353.1:n.*2352C=
ENST00000678546.1:c.*2048C= ENSP00000503062.1:n.*2048C=
ENST00000678548.1:c.*2242C= ENSP00000503934.1:n.*2242C=
ENST00000678626.1:n.1939C=
ENST00000678739.1:c.*2269C= ENSP00000503806.1:n.*2269C=
ENST00000678833.1:c.*1855C= ENSP00000503893.1:n.*1855C=
ENST00000679023.1:c.1941C= ENSP00000503718.1:p.Asp647=
ENST00000679076.1:c.1722C=
ENST00000679111.1:c.*859C= ENSP00000504257.1:n.*859C=
ENST00000679189.1:c.1752C= ENSP00000503356.1:p.Asp584=
ENST00000341012.11:c.1941C= ENSP00000343034.7:p.Asp647=
ENST00000372220.4:c.966C= ENSP00000361294.4:p.Asp322=
ENST00000372228.7:c.2169C= ENSP00000361302.3:p.Asp723=
ENST00000402686.7:c.2103C= ENSP00000385797.3:p.Asp701=
ENST00000404875.6:c.1752C= ENSP00000384531.2:p.Asp584=
ENST00000423007.5:c.2103C= ENSP00000404119.1:p.Asp701=
ENST00000485278.5:n.2653C=
NM_001077365.1:c.2103C= NP_001070833.1:p.Asp701=
NM_001077366.1:c.1941C= NP_001070834.1:p.Asp647=
NM_001136113.1:c.2103C= NP_001129585.1:p.Asp701=
NM_001136114.1:c.1752C= NP_001129586.1:p.Asp584=
NM_007171.3:c.2169C= NP_009102.3:p.Asp723=
XM_005272156.1:c.2169C= XP_005272213.1:p.Asp723=
XM_005272158.1:c.2007C= XP_005272215.1:p.Asp669=
XM_005272159.1:c.1818C= XP_005272216.1:p.Asp606=
XM_005272162.1:c.972C= XP_005272219.1:p.Asp324=
XM_006716932.1:c.1818C= XP_006716995.1:p.Asp606=
XM_011518140.1:c.2022C= XP_011516442.1:p.Asp674=
XM_011518141.1:c.1956C= XP_011516443.1:p.Asp652=
XM_011518142.1:c.1860C= XP_011516444.1:p.Asp620=
XM_011518143.1:c.1854C= XP_011516445.1:p.Asp618=
XM_011518145.1:c.1713C= XP_011516447.1:p.Asp571=
XM_011518147.1:c.1041C= XP_011516449.1:p.Asp347=
XR_929703.1:n.2345C=
NM_001353193.1:c.2169C= NP_001340122.1:p.Asp723=
NM_001353194.1:c.1941C= NP_001340123.1:p.Asp647=
NM_001353195.1:c.1752C= NP_001340124.1:p.Asp584=
NM_001353196.1:c.2013C= NP_001340125.1:p.Asp671=
NM_001353197.1:c.2007C= NP_001340126.1:p.Asp669=
NM_001353198.1:c.2007C= NP_001340127.1:p.Asp669=
NM_001353199.1:c.1818C= NP_001340128.1:p.Asp606=
NM_001353200.1:c.1647C= NP_001340129.1:p.Asp549=
NR_148391.1:n.2153C=
NR_148392.1:n.2371C=
NR_148393.1:n.2292C=
NR_148394.1:n.2046C=
NR_148395.1:n.2444C=
NR_148396.1:n.2078C=
NR_148397.1:n.2203C=
NR_148398.1:n.2158C=
NR_148399.1:n.2684C=
NR_148400.1:n.2283C=
XM_005272162.3:c.972C= XP_005272219.1:p.Asp324=
XM_006716932.2:c.1818C= XP_006716995.1:p.Asp606=
XM_011518140.2:c.2022C= XP_011516442.1:p.Asp674=
XM_011518141.2:c.1956C= XP_011516443.1:p.Asp652=
XM_011518142.2:c.1860C= XP_011516444.1:p.Asp620=
XM_011518143.2:c.1854C= XP_011516445.1:p.Asp618=
XM_011518145.2:c.1713C= XP_011516447.1:p.Asp571=
XM_017014205.2:c.972C= XP_016869694.1:p.Asp324=
XM_024447380.1:c.972C= XP_024303148.1:p.Asp324=
XM_024447381.1:c.1278C= XP_024303149.1:p.Asp426=
XM_024447382.1:c.972C= XP_024303150.1:p.Asp324=
XR_001746160.2:n.2273C=
XR_001746162.2:n.2478C=
XR_001746164.1:n.2195C=
XR_001746166.2:n.2490C=
NM_001077365.2:c.2103C= MANE Select NP_001070833.1:p.Asp701=
NM_001077366.2:c.1941C= NP_001070834.1:p.Asp647=
NM_001136113.2:c.2103C= NP_001129585.1:p.Asp701=
NM_001136114.2:c.1752C= NP_001129586.1:p.Asp584=
NM_001353193.2:c.2169C= NP_001340122.2:p.Asp723=
NM_001353194.2:c.1941C= NP_001340123.1:p.Asp647=
NM_001353195.2:c.1752C= NP_001340124.1:p.Asp584=
NM_001353196.2:c.2013C= NP_001340125.1:p.Asp671=
NM_001353197.2:c.2007C= NP_001340126.2:p.Asp669=
NM_001353198.2:c.2007C= NP_001340127.2:p.Asp669=
NM_001353199.2:c.1818C= NP_001340128.2:p.Asp606=
NM_001353200.2:c.1647C= NP_001340129.1:p.Asp549=
NM_001374689.1:c.2091C= NP_001361618.1:p.Asp697=
NM_001374690.1:c.1884C= NP_001361619.1:p.Asp628=
NM_001374691.1:c.1752C= NP_001361620.1:p.Asp584=
NM_001374692.1:c.1752C= NP_001361621.1:p.Asp584=
NM_001374693.1:c.1752C= NP_001361622.1:p.Asp584=
NM_001374695.1:c.1713C= NP_001361624.1:p.Asp571=
NM_007171.4:c.2169C= NP_009102.4:p.Asp723=
NR_148391.2:n.2137C=
NR_148392.2:n.2355C=
NR_148393.2:n.2276C=
NR_148394.2:n.2030C=
NR_148395.2:n.2428C=
NR_148396.2:n.2062C=
NR_148397.2:n.2187C=
NR_148398.2:n.2142C=
NR_148399.2:n.2668C=
NR_148400.2:n.2267C=