Canonical Allele Identifier: CA1881758310
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131522188C= , CM000671.2:g.131522188C= GRCh38
NC_000009.11:g.134397575C= , CM000671.1:g.134397575C= GRCh37
NC_000009.10:g.133387396C= NCBI36
NG_008896.1:g.24287C=
NG_008896.2:g.24287C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1805C= ENSP00000343034.7:p.Pro602=
ENST00000404875.7:n.2507C=
ENST00000423007.6:c.2024C= ENSP00000404119.2:p.Pro675=
ENST00000677295.2:c.*2311C= ENSP00000504346.2:n.*2311C=
ENST00000678264.2:c.*2150C= ENSP00000503157.2:n.*2150C=
ENST00000682070.1:n.2291-14C=
ENST00000682813.1:n.2371C=
ENST00000683392.1:n.4573-14C=
ENST00000683712.1:n.2372C=
ENST00000683900.1:n.3867C=
ENST00000684062.1:n.2633C=
ENST00000684579.1:n.3813C=
ENST00000684679.1:n.1194C=
ENST00000341012.12:c.1805C= ENSP00000343034.7:p.Pro602=
ENST00000372220.5:c.836C= ENSP00000361294.5:p.Pro279=
ENST00000372228.9:c.2033C= ENSP00000361302.3:p.Pro678=
ENST00000402686.8:c.1967C= MANE Select ENSP00000385797.4:p.Pro656=
ENST00000676640.1:c.1967C= ENSP00000503281.1:p.Pro656=
ENST00000676803.1:c.1028C= ENSP00000503093.1:p.Pro343=
ENST00000676835.1:c.*1182C= ENSP00000502911.1:n.*1182C=
ENST00000677029.1:c.1511C= ENSP00000502936.1:p.Pro504=
ENST00000677099.1:c.*1677C= ENSP00000504553.1:n.*1677C=
ENST00000677216.1:c.1616C= ENSP00000503772.1:p.Pro539=
ENST00000677221.1:n.992C=
ENST00000677295.1:c.*1203-14C= ENSP00000504346.1:n.*1203-14C=
ENST00000677444.1:c.1912C=
ENST00000677586.1:n.1334C=
ENST00000677626.1:c.1616C= ENSP00000503552.1:p.Pro539=
ENST00000677853.1:c.*975C= ENSP00000503488.1:n.*975C=
ENST00000678202.1:n.1126C=
ENST00000678264.1:c.*1344C= ENSP00000503157.1:n.*1344C=
ENST00000678303.1:c.1877C= ENSP00000503696.1:p.Pro626=
ENST00000678366.1:c.*2216C= ENSP00000504353.1:n.*2216C=
ENST00000678546.1:c.*1912C= ENSP00000503062.1:n.*1912C=
ENST00000678548.1:c.*2106C= ENSP00000503934.1:n.*2106C=
ENST00000678626.1:n.1803C=
ENST00000678739.1:c.*2147-14C= ENSP00000503806.1:n.*2147-14C=
ENST00000678833.1:c.*1719C= ENSP00000503893.1:n.*1719C=
ENST00000679023.1:c.1805C= ENSP00000503718.1:p.Pro602=
ENST00000679076.1:c.1586C=
ENST00000679111.1:c.*723C= ENSP00000504257.1:n.*723C=
ENST00000679189.1:c.1616C= ENSP00000503356.1:p.Pro539=
ENST00000341012.11:c.1805C= ENSP00000343034.7:p.Pro602=
ENST00000372220.4:c.830C= ENSP00000361294.4:p.Pro277=
ENST00000372228.7:c.2033C= ENSP00000361302.3:p.Pro678=
ENST00000402686.7:c.1967C= ENSP00000385797.3:p.Pro656=
ENST00000404875.6:c.1616C= ENSP00000384531.2:p.Pro539=
ENST00000423007.5:c.1967C= ENSP00000404119.1:p.Pro656=
ENST00000485278.5:n.2517C=
ENST00000494883.1:n.510C=
NM_001077365.1:c.1967C= NP_001070833.1:p.Pro656=
NM_001077366.1:c.1805C= NP_001070834.1:p.Pro602=
NM_001136113.1:c.1967C= NP_001129585.1:p.Pro656=
NM_001136114.1:c.1616C= NP_001129586.1:p.Pro539=
NM_007171.3:c.2033C= NP_009102.3:p.Pro678=
XM_005272156.1:c.2033C= XP_005272213.1:p.Pro678=
XM_005272158.1:c.1871C= XP_005272215.1:p.Pro624=
XM_005272159.1:c.1682C= XP_005272216.1:p.Pro561=
XM_005272162.1:c.836C= XP_005272219.1:p.Pro279=
XM_006716932.1:c.1682C= XP_006716995.1:p.Pro561=
XM_011518140.1:c.1886C= XP_011516442.1:p.Pro629=
XM_011518141.1:c.1820C= XP_011516443.1:p.Pro607=
XM_011518142.1:c.1724C= XP_011516444.1:p.Pro575=
XM_011518143.1:c.1718C= XP_011516445.1:p.Pro573=
XM_011518145.1:c.1577C= XP_011516447.1:p.Pro526=
XM_011518147.1:c.905C= XP_011516449.1:p.Pro302=
XR_929703.1:n.2209C=
NM_001353193.1:c.2033C= NP_001340122.1:p.Pro678=
NM_001353194.1:c.1805C= NP_001340123.1:p.Pro602=
NM_001353195.1:c.1616C= NP_001340124.1:p.Pro539=
NM_001353196.1:c.1877C= NP_001340125.1:p.Pro626=
NM_001353197.1:c.1871C= NP_001340126.1:p.Pro624=
NM_001353198.1:c.1871C= NP_001340127.1:p.Pro624=
NM_001353199.1:c.1682C= NP_001340128.1:p.Pro561=
NM_001353200.1:c.1511C= NP_001340129.1:p.Pro504=
NR_148391.1:n.2017C=
NR_148392.1:n.2235C=
NR_148393.1:n.2156C=
NR_148394.1:n.1910C=
NR_148395.1:n.2308C=
NR_148396.1:n.1942C=
NR_148397.1:n.2067C=
NR_148398.1:n.2022C=
NR_148399.1:n.2548C=
NR_148400.1:n.2147C=
XM_005272162.3:c.836C= XP_005272219.1:p.Pro279=
XM_006716932.2:c.1682C= XP_006716995.1:p.Pro561=
XM_011518140.2:c.1886C= XP_011516442.1:p.Pro629=
XM_011518141.2:c.1820C= XP_011516443.1:p.Pro607=
XM_011518142.2:c.1724C= XP_011516444.1:p.Pro575=
XM_011518143.2:c.1718C= XP_011516445.1:p.Pro573=
XM_011518145.2:c.1577C= XP_011516447.1:p.Pro526=
XM_017014205.2:c.836C= XP_016869694.1:p.Pro279=
XM_024447380.1:c.836C= XP_024303148.1:p.Pro279=
XM_024447381.1:c.1142C= XP_024303149.1:p.Pro381=
XM_024447382.1:c.836C= XP_024303150.1:p.Pro279=
XR_001746160.2:n.2137C=
XR_001746162.2:n.2342C=
XR_001746164.1:n.2059C=
XR_001746166.2:n.2354C=
NM_001077365.2:c.1967C= MANE Select NP_001070833.1:p.Pro656=
NM_001077366.2:c.1805C= NP_001070834.1:p.Pro602=
NM_001136113.2:c.1967C= NP_001129585.1:p.Pro656=
NM_001136114.2:c.1616C= NP_001129586.1:p.Pro539=
NM_001353193.2:c.2033C= NP_001340122.2:p.Pro678=
NM_001353194.2:c.1805C= NP_001340123.1:p.Pro602=
NM_001353195.2:c.1616C= NP_001340124.1:p.Pro539=
NM_001353196.2:c.1877C= NP_001340125.1:p.Pro626=
NM_001353197.2:c.1871C= NP_001340126.2:p.Pro624=
NM_001353198.2:c.1871C= NP_001340127.2:p.Pro624=
NM_001353199.2:c.1682C= NP_001340128.2:p.Pro561=
NM_001353200.2:c.1511C= NP_001340129.1:p.Pro504=
NM_001374689.1:c.1955C= NP_001361618.1:p.Pro652=
NM_001374690.1:c.1748C= NP_001361619.1:p.Pro583=
NM_001374691.1:c.1616C= NP_001361620.1:p.Pro539=
NM_001374692.1:c.1616C= NP_001361621.1:p.Pro539=
NM_001374693.1:c.1616C= NP_001361622.1:p.Pro539=
NM_001374695.1:c.1577C= NP_001361624.1:p.Pro526=
NM_007171.4:c.2033C= NP_009102.4:p.Pro678=
NR_148391.2:n.2001C=
NR_148392.2:n.2219C=
NR_148393.2:n.2140C=
NR_148394.2:n.1894C=
NR_148395.2:n.2292C=
NR_148396.2:n.1926C=
NR_148397.2:n.2051C=
NR_148398.2:n.2006C=
NR_148399.2:n.2532C=
NR_148400.2:n.2131C=