Canonical Allele Identifier: CA1881760473
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523065C= , CM000671.2:g.131523065C= GRCh38
NC_000009.11:g.134398452C= , CM000671.1:g.134398452C= GRCh37
NC_000009.10:g.133388273C= NCBI36
NG_008896.1:g.25164C=
NG_008896.2:g.25164C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1975C= ENSP00000343034.7:p.Arg659=
ENST00000404875.7:n.2677C=
ENST00000423007.6:c.2194C= ENSP00000404119.2:p.Arg732=
ENST00000677295.2:c.*2481C= ENSP00000504346.2:n.*2481C=
ENST00000678264.2:c.*2320C= ENSP00000503157.2:n.*2320C=
ENST00000682070.1:n.2447C=
ENST00000682639.1:c.134C=
ENST00000682813.1:n.2534C=
ENST00000683231.1:c.134C=
ENST00000683392.1:n.4729C=
ENST00000683712.1:n.2542C=
ENST00000683900.1:n.4037C=
ENST00000684062.1:n.2803C=
ENST00000684399.1:c.134C=
ENST00000684579.1:n.3983C=
ENST00000341012.12:c.1975C= ENSP00000343034.7:p.Arg659=
ENST00000372220.5:c.1006C= ENSP00000361294.5:p.Arg336=
ENST00000372228.9:c.2203C= ENSP00000361302.3:p.Arg735=
ENST00000402686.8:c.2137C= MANE Select ENSP00000385797.4:p.Arg713=
ENST00000676640.1:c.2137C= ENSP00000503281.1:p.Arg713=
ENST00000676803.1:c.1198C= ENSP00000503093.1:p.Arg400=
ENST00000676835.1:c.*1352C= ENSP00000502911.1:n.*1352C=
ENST00000677029.1:c.1681C= ENSP00000502936.1:p.Arg561=
ENST00000677099.1:c.*1847C= ENSP00000504553.1:n.*1847C=
ENST00000677216.1:c.1786C= ENSP00000503772.1:p.Arg596=
ENST00000677295.1:c.*1359C= ENSP00000504346.1:n.*1359C=
ENST00000677444.1:c.2082C=
ENST00000677586.1:n.1504C=
ENST00000677626.1:c.1786C= ENSP00000503552.1:p.Arg596=
ENST00000677853.1:c.*1145C= ENSP00000503488.1:n.*1145C=
ENST00000678264.1:c.*1514C= ENSP00000503157.1:n.*1514C=
ENST00000678303.1:c.2047C= ENSP00000503696.1:p.Arg683=
ENST00000678366.1:c.*2386C= ENSP00000504353.1:n.*2386C=
ENST00000678546.1:c.*2082C= ENSP00000503062.1:n.*2082C=
ENST00000678548.1:c.*2276C= ENSP00000503934.1:n.*2276C=
ENST00000678626.1:n.1973C=
ENST00000678739.1:c.*2303C= ENSP00000503806.1:n.*2303C=
ENST00000678833.1:c.*1889C= ENSP00000503893.1:n.*1889C=
ENST00000679023.1:c.1975C= ENSP00000503718.1:p.Arg659=
ENST00000679076.1:c.1756C=
ENST00000679111.1:c.*893C= ENSP00000504257.1:n.*893C=
ENST00000679189.1:c.1786C= ENSP00000503356.1:p.Arg596=
ENST00000341012.11:c.1975C= ENSP00000343034.7:p.Arg659=
ENST00000372220.4:c.1000C= ENSP00000361294.4:p.Arg334=
ENST00000372228.7:c.2203C= ENSP00000361302.3:p.Arg735=
ENST00000402686.7:c.2137C= ENSP00000385797.3:p.Arg713=
ENST00000404875.6:c.1786C= ENSP00000384531.2:p.Arg596=
ENST00000423007.5:c.2137C= ENSP00000404119.1:p.Arg713=
ENST00000485278.5:n.2687C=
NM_001077365.1:c.2137C= NP_001070833.1:p.Arg713=
NM_001077366.1:c.1975C= NP_001070834.1:p.Arg659=
NM_001136113.1:c.2137C= NP_001129585.1:p.Arg713=
NM_001136114.1:c.1786C= NP_001129586.1:p.Arg596=
NM_007171.3:c.2203C= NP_009102.3:p.Arg735=
XM_005272156.1:c.2203C= XP_005272213.1:p.Arg735=
XM_005272158.1:c.2041C= XP_005272215.1:p.Arg681=
XM_005272159.1:c.1852C= XP_005272216.1:p.Arg618=
XM_005272162.1:c.1006C= XP_005272219.1:p.Arg336=
XM_006716932.1:c.1852C= XP_006716995.1:p.Arg618=
XM_011518140.1:c.2056C= XP_011516442.1:p.Arg686=
XM_011518141.1:c.1990C= XP_011516443.1:p.Arg664=
XM_011518142.1:c.1894C= XP_011516444.1:p.Arg632=
XM_011518143.1:c.1888C= XP_011516445.1:p.Arg630=
XM_011518145.1:c.1747C= XP_011516447.1:p.Arg583=
XM_011518147.1:c.1075C= XP_011516449.1:p.Arg359=
XR_929703.1:n.2379C=
NM_001353193.1:c.2203C= NP_001340122.1:p.Arg735=
NM_001353194.1:c.1975C= NP_001340123.1:p.Arg659=
NM_001353195.1:c.1786C= NP_001340124.1:p.Arg596=
NM_001353196.1:c.2047C= NP_001340125.1:p.Arg683=
NM_001353197.1:c.2041C= NP_001340126.1:p.Arg681=
NM_001353198.1:c.2041C= NP_001340127.1:p.Arg681=
NM_001353199.1:c.1852C= NP_001340128.1:p.Arg618=
NM_001353200.1:c.1681C= NP_001340129.1:p.Arg561=
NR_148391.1:n.2187C=
NR_148392.1:n.2405C=
NR_148393.1:n.2326C=
NR_148394.1:n.2080C=
NR_148395.1:n.2478C=
NR_148396.1:n.2112C=
NR_148397.1:n.2237C=
NR_148398.1:n.2192C=
NR_148399.1:n.2718C=
NR_148400.1:n.2317C=
XM_005272162.3:c.1006C= XP_005272219.1:p.Arg336=
XM_006716932.2:c.1852C= XP_006716995.1:p.Arg618=
XM_011518140.2:c.2056C= XP_011516442.1:p.Arg686=
XM_011518141.2:c.1990C= XP_011516443.1:p.Arg664=
XM_011518142.2:c.1894C= XP_011516444.1:p.Arg632=
XM_011518143.2:c.1888C= XP_011516445.1:p.Arg630=
XM_011518145.2:c.1747C= XP_011516447.1:p.Arg583=
XM_017014205.2:c.1006C= XP_016869694.1:p.Arg336=
XM_024447380.1:c.1006C= XP_024303148.1:p.Arg336=
XM_024447381.1:c.1312C= XP_024303149.1:p.Arg438=
XM_024447382.1:c.1006C= XP_024303150.1:p.Arg336=
XR_001746160.2:n.2307C=
XR_001746162.2:n.2512C=
XR_001746164.1:n.2229C=
XR_001746166.2:n.2524C=
NM_001077365.2:c.2137C= MANE Select NP_001070833.1:p.Arg713=
NM_001077366.2:c.1975C= NP_001070834.1:p.Arg659=
NM_001136113.2:c.2137C= NP_001129585.1:p.Arg713=
NM_001136114.2:c.1786C= NP_001129586.1:p.Arg596=
NM_001353193.2:c.2203C= NP_001340122.2:p.Arg735=
NM_001353194.2:c.1975C= NP_001340123.1:p.Arg659=
NM_001353195.2:c.1786C= NP_001340124.1:p.Arg596=
NM_001353196.2:c.2047C= NP_001340125.1:p.Arg683=
NM_001353197.2:c.2041C= NP_001340126.2:p.Arg681=
NM_001353198.2:c.2041C= NP_001340127.2:p.Arg681=
NM_001353199.2:c.1852C= NP_001340128.2:p.Arg618=
NM_001353200.2:c.1681C= NP_001340129.1:p.Arg561=
NM_001374689.1:c.2125C= NP_001361618.1:p.Arg709=
NM_001374690.1:c.1918C= NP_001361619.1:p.Arg640=
NM_001374691.1:c.1786C= NP_001361620.1:p.Arg596=
NM_001374692.1:c.1786C= NP_001361621.1:p.Arg596=
NM_001374693.1:c.1786C= NP_001361622.1:p.Arg596=
NM_001374695.1:c.1747C= NP_001361624.1:p.Arg583=
NM_007171.4:c.2203C= NP_009102.4:p.Arg735=
NR_148391.2:n.2171C=
NR_148392.2:n.2389C=
NR_148393.2:n.2310C=
NR_148394.2:n.2064C=
NR_148395.2:n.2462C=
NR_148396.2:n.2096C=
NR_148397.2:n.2221C=
NR_148398.2:n.2176C=
NR_148399.2:n.2702C=
NR_148400.2:n.2301C=