Canonical Allele Identifier: CA1881760467
Gene: POMT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.131523060C= , CM000671.2:g.131523060C= GRCh38
NC_000009.11:g.134398447C= , CM000671.1:g.134398447C= GRCh37
NC_000009.10:g.133388268C= NCBI36
NG_008896.1:g.25159C=
NG_008896.2:g.25159C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000341012.13:c.1970C= ENSP00000343034.7:p.Ala657=
ENST00000404875.7:n.2672C=
ENST00000423007.6:c.2189C= ENSP00000404119.2:p.Ala730=
ENST00000677295.2:c.*2476C= ENSP00000504346.2:n.*2476C=
ENST00000678264.2:c.*2315C= ENSP00000503157.2:n.*2315C=
ENST00000682070.1:n.2442C=
ENST00000682639.1:c.129C=
ENST00000682813.1:n.2529C=
ENST00000683231.1:c.129C=
ENST00000683392.1:n.4724C=
ENST00000683712.1:n.2537C=
ENST00000683900.1:n.4032C=
ENST00000684062.1:n.2798C=
ENST00000684399.1:c.129C=
ENST00000684579.1:n.3978C=
ENST00000341012.12:c.1970C= ENSP00000343034.7:p.Ala657=
ENST00000372220.5:c.1001C= ENSP00000361294.5:p.Ala334=
ENST00000372228.9:c.2198C= ENSP00000361302.3:p.Ala733=
ENST00000402686.8:c.2132C= MANE Select ENSP00000385797.4:p.Ala711=
ENST00000676640.1:c.2132C= ENSP00000503281.1:p.Ala711=
ENST00000676803.1:c.1193C= ENSP00000503093.1:p.Ala398=
ENST00000676835.1:c.*1347C= ENSP00000502911.1:n.*1347C=
ENST00000677029.1:c.1676C= ENSP00000502936.1:p.Ala559=
ENST00000677099.1:c.*1842C= ENSP00000504553.1:n.*1842C=
ENST00000677216.1:c.1781C= ENSP00000503772.1:p.Ala594=
ENST00000677295.1:c.*1354C= ENSP00000504346.1:n.*1354C=
ENST00000677444.1:c.2077C=
ENST00000677586.1:n.1499C=
ENST00000677626.1:c.1781C= ENSP00000503552.1:p.Ala594=
ENST00000677853.1:c.*1140C= ENSP00000503488.1:n.*1140C=
ENST00000678264.1:c.*1509C= ENSP00000503157.1:n.*1509C=
ENST00000678303.1:c.2042C= ENSP00000503696.1:p.Ala681=
ENST00000678366.1:c.*2381C= ENSP00000504353.1:n.*2381C=
ENST00000678546.1:c.*2077C= ENSP00000503062.1:n.*2077C=
ENST00000678548.1:c.*2271C= ENSP00000503934.1:n.*2271C=
ENST00000678626.1:n.1968C=
ENST00000678739.1:c.*2298C= ENSP00000503806.1:n.*2298C=
ENST00000678833.1:c.*1884C= ENSP00000503893.1:n.*1884C=
ENST00000679023.1:c.1970C= ENSP00000503718.1:p.Ala657=
ENST00000679076.1:c.1751C=
ENST00000679111.1:c.*888C= ENSP00000504257.1:n.*888C=
ENST00000679189.1:c.1781C= ENSP00000503356.1:p.Ala594=
ENST00000341012.11:c.1970C= ENSP00000343034.7:p.Ala657=
ENST00000372220.4:c.995C= ENSP00000361294.4:p.Ala332=
ENST00000372228.7:c.2198C= ENSP00000361302.3:p.Ala733=
ENST00000402686.7:c.2132C= ENSP00000385797.3:p.Ala711=
ENST00000404875.6:c.1781C= ENSP00000384531.2:p.Ala594=
ENST00000423007.5:c.2132C= ENSP00000404119.1:p.Ala711=
ENST00000485278.5:n.2682C=
NM_001077365.1:c.2132C= NP_001070833.1:p.Ala711=
NM_001077366.1:c.1970C= NP_001070834.1:p.Ala657=
NM_001136113.1:c.2132C= NP_001129585.1:p.Ala711=
NM_001136114.1:c.1781C= NP_001129586.1:p.Ala594=
NM_007171.3:c.2198C= NP_009102.3:p.Ala733=
XM_005272156.1:c.2198C= XP_005272213.1:p.Ala733=
XM_005272158.1:c.2036C= XP_005272215.1:p.Ala679=
XM_005272159.1:c.1847C= XP_005272216.1:p.Ala616=
XM_005272162.1:c.1001C= XP_005272219.1:p.Ala334=
XM_006716932.1:c.1847C= XP_006716995.1:p.Ala616=
XM_011518140.1:c.2051C= XP_011516442.1:p.Ala684=
XM_011518141.1:c.1985C= XP_011516443.1:p.Ala662=
XM_011518142.1:c.1889C= XP_011516444.1:p.Ala630=
XM_011518143.1:c.1883C= XP_011516445.1:p.Ala628=
XM_011518145.1:c.1742C= XP_011516447.1:p.Ala581=
XM_011518147.1:c.1070C= XP_011516449.1:p.Ala357=
XR_929703.1:n.2374C=
NM_001353193.1:c.2198C= NP_001340122.1:p.Ala733=
NM_001353194.1:c.1970C= NP_001340123.1:p.Ala657=
NM_001353195.1:c.1781C= NP_001340124.1:p.Ala594=
NM_001353196.1:c.2042C= NP_001340125.1:p.Ala681=
NM_001353197.1:c.2036C= NP_001340126.1:p.Ala679=
NM_001353198.1:c.2036C= NP_001340127.1:p.Ala679=
NM_001353199.1:c.1847C= NP_001340128.1:p.Ala616=
NM_001353200.1:c.1676C= NP_001340129.1:p.Ala559=
NR_148391.1:n.2182C=
NR_148392.1:n.2400C=
NR_148393.1:n.2321C=
NR_148394.1:n.2075C=
NR_148395.1:n.2473C=
NR_148396.1:n.2107C=
NR_148397.1:n.2232C=
NR_148398.1:n.2187C=
NR_148399.1:n.2713C=
NR_148400.1:n.2312C=
XM_005272162.3:c.1001C= XP_005272219.1:p.Ala334=
XM_006716932.2:c.1847C= XP_006716995.1:p.Ala616=
XM_011518140.2:c.2051C= XP_011516442.1:p.Ala684=
XM_011518141.2:c.1985C= XP_011516443.1:p.Ala662=
XM_011518142.2:c.1889C= XP_011516444.1:p.Ala630=
XM_011518143.2:c.1883C= XP_011516445.1:p.Ala628=
XM_011518145.2:c.1742C= XP_011516447.1:p.Ala581=
XM_017014205.2:c.1001C= XP_016869694.1:p.Ala334=
XM_024447380.1:c.1001C= XP_024303148.1:p.Ala334=
XM_024447381.1:c.1307C= XP_024303149.1:p.Ala436=
XM_024447382.1:c.1001C= XP_024303150.1:p.Ala334=
XR_001746160.2:n.2302C=
XR_001746162.2:n.2507C=
XR_001746164.1:n.2224C=
XR_001746166.2:n.2519C=
NM_001077365.2:c.2132C= MANE Select NP_001070833.1:p.Ala711=
NM_001077366.2:c.1970C= NP_001070834.1:p.Ala657=
NM_001136113.2:c.2132C= NP_001129585.1:p.Ala711=
NM_001136114.2:c.1781C= NP_001129586.1:p.Ala594=
NM_001353193.2:c.2198C= NP_001340122.2:p.Ala733=
NM_001353194.2:c.1970C= NP_001340123.1:p.Ala657=
NM_001353195.2:c.1781C= NP_001340124.1:p.Ala594=
NM_001353196.2:c.2042C= NP_001340125.1:p.Ala681=
NM_001353197.2:c.2036C= NP_001340126.2:p.Ala679=
NM_001353198.2:c.2036C= NP_001340127.2:p.Ala679=
NM_001353199.2:c.1847C= NP_001340128.2:p.Ala616=
NM_001353200.2:c.1676C= NP_001340129.1:p.Ala559=
NM_001374689.1:c.2120C= NP_001361618.1:p.Ala707=
NM_001374690.1:c.1913C= NP_001361619.1:p.Ala638=
NM_001374691.1:c.1781C= NP_001361620.1:p.Ala594=
NM_001374692.1:c.1781C= NP_001361621.1:p.Ala594=
NM_001374693.1:c.1781C= NP_001361622.1:p.Ala594=
NM_001374695.1:c.1742C= NP_001361624.1:p.Ala581=
NM_007171.4:c.2198C= NP_009102.4:p.Ala733=
NR_148391.2:n.2166C=
NR_148392.2:n.2384C=
NR_148393.2:n.2305C=
NR_148394.2:n.2059C=
NR_148395.2:n.2457C=
NR_148396.2:n.2091C=
NR_148397.2:n.2216C=
NR_148398.2:n.2171C=
NR_148399.2:n.2697C=
NR_148400.2:n.2296C=