Canonical Allele Identifier: CA375314143

Gene: POMT1

Linked Data

• MyVariant Identifiers: chr9:g.134397445C>G (hg19) ; chr9:g.131522058C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522058C>G , CM000671.2:g.131522058C>G	GRCh38
NC_000009.11:g.134397445C>G , CM000671.1:g.134397445C>G	GRCh37
NC_000009.10:g.133387266C>G	NCBI36
NG_008896.1:g.24157C>G
NG_008896.2:g.24157C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.1675C>G	ENSP00000343034.7:p.Arg559Gly
ENST00000404875.7:n.2377C>G
ENST00000423007.6:c.1894C>G	ENSP00000404119.2:p.Arg632Gly
ENST00000677295.2:c.*2181C>G	ENSP00000504346.2:n.*2181C>G
ENST00000678264.2:c.*2020C>G	ENSP00000503157.2:n.*2020C>G
ENST00000682070.1:n.2291-144C>G
ENST00000682813.1:n.2241C>G
ENST00000683392.1:n.4573-144C>G
ENST00000683712.1:n.2242C>G
ENST00000683900.1:n.3737C>G
ENST00000684062.1:n.2503C>G
ENST00000684579.1:n.3683C>G
ENST00000684679.1:n.1064C>G
ENST00000341012.12:c.1675C>G	ENSP00000343034.7:p.Arg559Gly
ENST00000372220.5:c.706C>G	ENSP00000361294.5:p.Arg236Gly
ENST00000372228.9:c.1903C>G	ENSP00000361302.3:p.Arg635Gly
ENST00000402686.8:c.1837C>G MANE Select	ENSP00000385797.4:p.Arg613Gly
ENST00000676640.1:c.1837C>G	ENSP00000503281.1:p.Arg613Gly
ENST00000676803.1:c.898C>G	ENSP00000503093.1:p.Arg300Gly
ENST00000676835.1:c.*1052C>G	ENSP00000502911.1:n.*1052C>G
ENST00000677029.1:c.1381C>G	ENSP00000502936.1:p.Arg461Gly
ENST00000677099.1:c.*1547C>G	ENSP00000504553.1:n.*1547C>G
ENST00000677216.1:c.1486C>G	ENSP00000503772.1:p.Arg496Gly
ENST00000677221.1:n.862C>G
ENST00000677295.1:c.*1203-144C>G	ENSP00000504346.1:n.*1203-144C>G
ENST00000677444.1:c.1782C>G
ENST00000677586.1:n.1204C>G
ENST00000677626.1:c.1486C>G	ENSP00000503552.1:p.Arg496Gly
ENST00000677853.1:c.*845C>G	ENSP00000503488.1:n.*845C>G
ENST00000678202.1:n.996C>G
ENST00000678264.1:c.*1214C>G	ENSP00000503157.1:n.*1214C>G
ENST00000678303.1:c.1747C>G	ENSP00000503696.1:p.Arg583Gly
ENST00000678366.1:c.*2086C>G	ENSP00000504353.1:n.*2086C>G
ENST00000678546.1:c.*1782C>G	ENSP00000503062.1:n.*1782C>G
ENST00000678548.1:c.*1976C>G	ENSP00000503934.1:n.*1976C>G
ENST00000678626.1:n.1673C>G
ENST00000678739.1:c.*2147-144C>G	ENSP00000503806.1:n.*2147-144C>G
ENST00000678833.1:c.*1589C>G	ENSP00000503893.1:n.*1589C>G
ENST00000679023.1:c.1675C>G	ENSP00000503718.1:p.Arg559Gly
ENST00000679076.1:c.1456C>G
ENST00000679111.1:c.*593C>G	ENSP00000504257.1:n.*593C>G
ENST00000679189.1:c.1486C>G	ENSP00000503356.1:p.Arg496Gly
ENST00000341012.11:c.1675C>G	ENSP00000343034.7:p.Arg559Gly
ENST00000372220.4:c.700C>G	ENSP00000361294.4:p.Arg234Gly
ENST00000372228.7:c.1903C>G	ENSP00000361302.3:p.Arg635Gly
ENST00000402686.7:c.1837C>G	ENSP00000385797.3:p.Arg613Gly
ENST00000404875.6:c.1486C>G	ENSP00000384531.2:p.Arg496Gly
ENST00000423007.5:c.1837C>G	ENSP00000404119.1:p.Arg613Gly
ENST00000485278.5:n.2387C>G
ENST00000494883.1:n.380C>G
NM_001077365.1:c.1837C>G	NP_001070833.1:p.Arg613Gly
NM_001077366.1:c.1675C>G	NP_001070834.1:p.Arg559Gly
NM_001136113.1:c.1837C>G	NP_001129585.1:p.Arg613Gly
NM_001136114.1:c.1486C>G	NP_001129586.1:p.Arg496Gly
NM_007171.3:c.1903C>G	NP_009102.3:p.Arg635Gly
XM_005272156.1:c.1903C>G	XP_005272213.1:p.Arg635Gly
XM_005272158.1:c.1741C>G	XP_005272215.1:p.Arg581Gly
XM_005272159.1:c.1552C>G	XP_005272216.1:p.Arg518Gly
XM_005272162.1:c.706C>G	XP_005272219.1:p.Arg236Gly
XM_006716932.1:c.1552C>G	XP_006716995.1:p.Arg518Gly
XM_011518140.1:c.1756C>G	XP_011516442.1:p.Arg586Gly
XM_011518141.1:c.1690C>G	XP_011516443.1:p.Arg564Gly
XM_011518142.1:c.1594C>G	XP_011516444.1:p.Arg532Gly
XM_011518143.1:c.1588C>G	XP_011516445.1:p.Arg530Gly
XM_011518145.1:c.1447C>G	XP_011516447.1:p.Arg483Gly
XM_011518147.1:c.775C>G	XP_011516449.1:p.Arg259Gly
XR_929703.1:n.2079C>G
NM_001353193.1:c.1903C>G	NP_001340122.1:p.Arg635Gly
NM_001353194.1:c.1675C>G	NP_001340123.1:p.Arg559Gly
NM_001353195.1:c.1486C>G	NP_001340124.1:p.Arg496Gly
NM_001353196.1:c.1747C>G	NP_001340125.1:p.Arg583Gly
NM_001353197.1:c.1741C>G	NP_001340126.1:p.Arg581Gly
NM_001353198.1:c.1741C>G	NP_001340127.1:p.Arg581Gly
NM_001353199.1:c.1552C>G	NP_001340128.1:p.Arg518Gly
NM_001353200.1:c.1381C>G	NP_001340129.1:p.Arg461Gly
NR_148391.1:n.1887C>G
NR_148392.1:n.2105C>G
NR_148393.1:n.2026C>G
NR_148394.1:n.1780C>G
NR_148395.1:n.2178C>G
NR_148396.1:n.1812C>G
NR_148397.1:n.1937C>G
NR_148398.1:n.1892C>G
NR_148399.1:n.2418C>G
NR_148400.1:n.2017C>G
XM_005272162.3:c.706C>G	XP_005272219.1:p.Arg236Gly
XM_006716932.2:c.1552C>G	XP_006716995.1:p.Arg518Gly
XM_011518140.2:c.1756C>G	XP_011516442.1:p.Arg586Gly
XM_011518141.2:c.1690C>G	XP_011516443.1:p.Arg564Gly
XM_011518142.2:c.1594C>G	XP_011516444.1:p.Arg532Gly
XM_011518143.2:c.1588C>G	XP_011516445.1:p.Arg530Gly
XM_011518145.2:c.1447C>G	XP_011516447.1:p.Arg483Gly
XM_017014205.2:c.706C>G	XP_016869694.1:p.Arg236Gly
XM_024447380.1:c.706C>G	XP_024303148.1:p.Arg236Gly
XM_024447381.1:c.1012C>G	XP_024303149.1:p.Arg338Gly
XM_024447382.1:c.706C>G	XP_024303150.1:p.Arg236Gly
XR_001746160.2:n.2007C>G
XR_001746162.2:n.2212C>G
XR_001746164.1:n.1929C>G
XR_001746166.2:n.2224C>G
NM_001077365.2:c.1837C>G MANE Select	NP_001070833.1:p.Arg613Gly
NM_001077366.2:c.1675C>G	NP_001070834.1:p.Arg559Gly
NM_001136113.2:c.1837C>G	NP_001129585.1:p.Arg613Gly
NM_001136114.2:c.1486C>G	NP_001129586.1:p.Arg496Gly
NM_001353193.2:c.1903C>G	NP_001340122.2:p.Arg635Gly
NM_001353194.2:c.1675C>G	NP_001340123.1:p.Arg559Gly
NM_001353195.2:c.1486C>G	NP_001340124.1:p.Arg496Gly
NM_001353196.2:c.1747C>G	NP_001340125.1:p.Arg583Gly
NM_001353197.2:c.1741C>G	NP_001340126.2:p.Arg581Gly
NM_001353198.2:c.1741C>G	NP_001340127.2:p.Arg581Gly
NM_001353199.2:c.1552C>G	NP_001340128.2:p.Arg518Gly
NM_001353200.2:c.1381C>G	NP_001340129.1:p.Arg461Gly
NM_001374689.1:c.1825C>G	NP_001361618.1:p.Arg609Gly
NM_001374690.1:c.1618C>G	NP_001361619.1:p.Arg540Gly
NM_001374691.1:c.1486C>G	NP_001361620.1:p.Arg496Gly
NM_001374692.1:c.1486C>G	NP_001361621.1:p.Arg496Gly
NM_001374693.1:c.1486C>G	NP_001361622.1:p.Arg496Gly
NM_001374695.1:c.1447C>G	NP_001361624.1:p.Arg483Gly
NM_007171.4:c.1903C>G	NP_009102.4:p.Arg635Gly
NR_148391.2:n.1871C>G
NR_148392.2:n.2089C>G
NR_148393.2:n.2010C>G
NR_148394.2:n.1764C>G
NR_148395.2:n.2162C>G
NR_148396.2:n.1796C>G
NR_148397.2:n.1921C>G
NR_148398.2:n.1876C>G
NR_148399.2:n.2402C>G
NR_148400.2:n.2001C>G