Canonical Allele Identifier: CA1881760001
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522970T= , CM000671.2:g.131522970T= GRCh38
NC_000009.11:g.134398357T= , CM000671.1:g.134398357T= GRCh37
NC_000009.10:g.133388178T= NCBI36
NG_008896.1:g.25069T=
NG_008896.2:g.25069T=

Transcript Alleles

HGVS Amino-acid change
ENST00000341012.13:c.1880T= ENSP00000343034.7:p.Val627=
ENST00000404875.7:n.2582T=
ENST00000423007.6:c.2099T= ENSP00000404119.2:p.Val700=
ENST00000677295.2:c.*2386T= ENSP00000504346.2:n.*2386T=
ENST00000678264.2:c.*2225T= ENSP00000503157.2:n.*2225T=
ENST00000682070.1:n.2352T=
ENST00000682639.1:c.39T=
ENST00000682813.1:n.2439T=
ENST00000683231.1:c.39T=
ENST00000683392.1:n.4634T=
ENST00000683712.1:n.2447T=
ENST00000683900.1:n.3942T=
ENST00000684062.1:n.2708T=
ENST00000684399.1:c.39T=
ENST00000684579.1:n.3888T=
ENST00000341012.12:c.1880T= ENSP00000343034.7:p.Val627=
ENST00000372220.5:c.911T= ENSP00000361294.5:p.Val304=
ENST00000372228.9:c.2108T= ENSP00000361302.3:p.Val703=
ENST00000402686.8:c.2042T= MANE Select ENSP00000385797.4:p.Val681=
ENST00000676640.1:c.2042T= ENSP00000503281.1:p.Val681=
ENST00000676803.1:c.1103T= ENSP00000503093.1:p.Val368=
ENST00000676835.1:c.*1257T= ENSP00000502911.1:n.*1257T=
ENST00000677029.1:c.1586T= ENSP00000502936.1:p.Val529=
ENST00000677099.1:c.*1752T= ENSP00000504553.1:n.*1752T=
ENST00000677216.1:c.1691T= ENSP00000503772.1:p.Val564=
ENST00000677221.1:n.1067T=
ENST00000677295.1:c.*1264T= ENSP00000504346.1:n.*1264T=
ENST00000677444.1:c.1987T=
ENST00000677586.1:n.1409T=
ENST00000677626.1:c.1691T= ENSP00000503552.1:p.Val564=
ENST00000677853.1:c.*1050T= ENSP00000503488.1:n.*1050T=
ENST00000678264.1:c.*1419T= ENSP00000503157.1:n.*1419T=
ENST00000678303.1:c.1952T= ENSP00000503696.1:p.Val651=
ENST00000678366.1:c.*2291T= ENSP00000504353.1:n.*2291T=
ENST00000678546.1:c.*1987T= ENSP00000503062.1:n.*1987T=
ENST00000678548.1:c.*2181T= ENSP00000503934.1:n.*2181T=
ENST00000678626.1:n.1878T=
ENST00000678739.1:c.*2208T= ENSP00000503806.1:n.*2208T=
ENST00000678833.1:c.*1794T= ENSP00000503893.1:n.*1794T=
ENST00000679023.1:c.1880T= ENSP00000503718.1:p.Val627=
ENST00000679076.1:c.1661T=
ENST00000679111.1:c.*798T= ENSP00000504257.1:n.*798T=
ENST00000679189.1:c.1691T= ENSP00000503356.1:p.Val564=
ENST00000341012.11:c.1880T= ENSP00000343034.7:p.Val627=
ENST00000372220.4:c.905T= ENSP00000361294.4:p.Val302=
ENST00000372228.7:c.2108T= ENSP00000361302.3:p.Val703=
ENST00000402686.7:c.2042T= ENSP00000385797.3:p.Val681=
ENST00000404875.6:c.1691T= ENSP00000384531.2:p.Val564=
ENST00000423007.5:c.2042T= ENSP00000404119.1:p.Val681=
ENST00000485278.5:n.2592T=
NM_001077365.1:c.2042T= NP_001070833.1:p.Val681=
NM_001077366.1:c.1880T= NP_001070834.1:p.Val627=
NM_001136113.1:c.2042T= NP_001129585.1:p.Val681=
NM_001136114.1:c.1691T= NP_001129586.1:p.Val564=
NM_007171.3:c.2108T= NP_009102.3:p.Val703=
XM_005272156.1:c.2108T= XP_005272213.1:p.Val703=
XM_005272158.1:c.1946T= XP_005272215.1:p.Val649=
XM_005272159.1:c.1757T= XP_005272216.1:p.Val586=
XM_005272162.1:c.911T= XP_005272219.1:p.Val304=
XM_006716932.1:c.1757T= XP_006716995.1:p.Val586=
XM_011518140.1:c.1961T= XP_011516442.1:p.Val654=
XM_011518141.1:c.1895T= XP_011516443.1:p.Val632=
XM_011518142.1:c.1799T= XP_011516444.1:p.Val600=
XM_011518143.1:c.1793T= XP_011516445.1:p.Val598=
XM_011518145.1:c.1652T= XP_011516447.1:p.Val551=
XM_011518147.1:c.980T= XP_011516449.1:p.Val327=
XR_929703.1:n.2284T=
NM_001353193.1:c.2108T= NP_001340122.1:p.Val703=
NM_001353194.1:c.1880T= NP_001340123.1:p.Val627=
NM_001353195.1:c.1691T= NP_001340124.1:p.Val564=
NM_001353196.1:c.1952T= NP_001340125.1:p.Val651=
NM_001353197.1:c.1946T= NP_001340126.1:p.Val649=
NM_001353198.1:c.1946T= NP_001340127.1:p.Val649=
NM_001353199.1:c.1757T= NP_001340128.1:p.Val586=
NM_001353200.1:c.1586T= NP_001340129.1:p.Val529=
NR_148391.1:n.2092T=
NR_148392.1:n.2310T=
NR_148393.1:n.2231T=
NR_148394.1:n.1985T=
NR_148395.1:n.2383T=
NR_148396.1:n.2017T=
NR_148397.1:n.2142T=
NR_148398.1:n.2097T=
NR_148399.1:n.2623T=
NR_148400.1:n.2222T=
XM_005272162.3:c.911T= XP_005272219.1:p.Val304=
XM_006716932.2:c.1757T= XP_006716995.1:p.Val586=
XM_011518140.2:c.1961T= XP_011516442.1:p.Val654=
XM_011518141.2:c.1895T= XP_011516443.1:p.Val632=
XM_011518142.2:c.1799T= XP_011516444.1:p.Val600=
XM_011518143.2:c.1793T= XP_011516445.1:p.Val598=
XM_011518145.2:c.1652T= XP_011516447.1:p.Val551=
XM_017014205.2:c.911T= XP_016869694.1:p.Val304=
XM_024447380.1:c.911T= XP_024303148.1:p.Val304=
XM_024447381.1:c.1217T= XP_024303149.1:p.Val406=
XM_024447382.1:c.911T= XP_024303150.1:p.Val304=
XR_001746160.2:n.2212T=
XR_001746162.2:n.2417T=
XR_001746164.1:n.2134T=
XR_001746166.2:n.2429T=
NM_001077365.2:c.2042T= MANE Select NP_001070833.1:p.Val681=
NM_001077366.2:c.1880T= NP_001070834.1:p.Val627=
NM_001136113.2:c.2042T= NP_001129585.1:p.Val681=
NM_001136114.2:c.1691T= NP_001129586.1:p.Val564=
NM_001353193.2:c.2108T= NP_001340122.2:p.Val703=
NM_001353194.2:c.1880T= NP_001340123.1:p.Val627=
NM_001353195.2:c.1691T= NP_001340124.1:p.Val564=
NM_001353196.2:c.1952T= NP_001340125.1:p.Val651=
NM_001353197.2:c.1946T= NP_001340126.2:p.Val649=
NM_001353198.2:c.1946T= NP_001340127.2:p.Val649=
NM_001353199.2:c.1757T= NP_001340128.2:p.Val586=
NM_001353200.2:c.1586T= NP_001340129.1:p.Val529=
NM_001374689.1:c.2030T= NP_001361618.1:p.Val677=
NM_001374690.1:c.1823T= NP_001361619.1:p.Val608=
NM_001374691.1:c.1691T= NP_001361620.1:p.Val564=
NM_001374692.1:c.1691T= NP_001361621.1:p.Val564=
NM_001374693.1:c.1691T= NP_001361622.1:p.Val564=
NM_001374695.1:c.1652T= NP_001361624.1:p.Val551=
NM_007171.4:c.2108T= NP_009102.4:p.Val703=
NR_148391.2:n.2076T=
NR_148392.2:n.2294T=
NR_148393.2:n.2215T=
NR_148394.2:n.1969T=
NR_148395.2:n.2367T=
NR_148396.2:n.2001T=
NR_148397.2:n.2126T=
NR_148398.2:n.2081T=
NR_148399.2:n.2607T=
NR_148400.2:n.2206T=