Canonical Allele Identifier: CA467424084

Gene: POMT1

Linked Data

• MyVariant Identifiers: chr9:g.134397555C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522168C>A , CM000671.2:g.131522168C>A	GRCh38
NC_000009.11:g.134397555C>A , CM000671.1:g.134397555C>A	GRCh37
NC_000009.10:g.133387376C>A	NCBI36
NG_008896.1:g.24267C>A
NG_008896.2:g.24267C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000341012.13:c.1785C>A	ENSP00000343034.7:p.Thr595=
ENST00000404875.7:n.2487C>A
ENST00000423007.6:c.2004C>A	ENSP00000404119.2:p.Thr668=
ENST00000677295.2:c.*2291C>A	ENSP00000504346.2:n.*2291C>A
ENST00000678264.2:c.*2130C>A	ENSP00000503157.2:n.*2130C>A
ENST00000682070.1:n.2291-34C>A
ENST00000682813.1:n.2351C>A
ENST00000683392.1:n.4573-34C>A
ENST00000683712.1:n.2352C>A
ENST00000683900.1:n.3847C>A
ENST00000684062.1:n.2613C>A
ENST00000684579.1:n.3793C>A
ENST00000684679.1:n.1174C>A
ENST00000341012.12:c.1785C>A	ENSP00000343034.7:p.Thr595=
ENST00000372220.5:c.816C>A	ENSP00000361294.5:p.Thr272=
ENST00000372228.9:c.2013C>A	ENSP00000361302.3:p.Thr671=
ENST00000402686.8:c.1947C>A MANE Select	ENSP00000385797.4:p.Thr649=
ENST00000676640.1:c.1947C>A	ENSP00000503281.1:p.Thr649=
ENST00000676803.1:c.1008C>A	ENSP00000503093.1:p.Thr336=
ENST00000676835.1:c.*1162C>A	ENSP00000502911.1:n.*1162C>A
ENST00000677029.1:c.1491C>A	ENSP00000502936.1:p.Thr497=
ENST00000677099.1:c.*1657C>A	ENSP00000504553.1:n.*1657C>A
ENST00000677216.1:c.1596C>A	ENSP00000503772.1:p.Thr532=
ENST00000677221.1:n.972C>A
ENST00000677295.1:c.*1203-34C>A	ENSP00000504346.1:n.*1203-34C>A
ENST00000677444.1:c.1892C>A
ENST00000677586.1:n.1314C>A
ENST00000677626.1:c.1596C>A	ENSP00000503552.1:p.Thr532=
ENST00000677853.1:c.*955C>A	ENSP00000503488.1:n.*955C>A
ENST00000678202.1:n.1106C>A
ENST00000678264.1:c.*1324C>A	ENSP00000503157.1:n.*1324C>A
ENST00000678303.1:c.1857C>A	ENSP00000503696.1:p.Thr619=
ENST00000678366.1:c.*2196C>A	ENSP00000504353.1:n.*2196C>A
ENST00000678546.1:c.*1892C>A	ENSP00000503062.1:n.*1892C>A
ENST00000678548.1:c.*2086C>A	ENSP00000503934.1:n.*2086C>A
ENST00000678626.1:n.1783C>A
ENST00000678739.1:c.*2147-34C>A	ENSP00000503806.1:n.*2147-34C>A
ENST00000678833.1:c.*1699C>A	ENSP00000503893.1:n.*1699C>A
ENST00000679023.1:c.1785C>A	ENSP00000503718.1:p.Thr595=
ENST00000679076.1:c.1566C>A
ENST00000679111.1:c.*703C>A	ENSP00000504257.1:n.*703C>A
ENST00000679189.1:c.1596C>A	ENSP00000503356.1:p.Thr532=
ENST00000341012.11:c.1785C>A	ENSP00000343034.7:p.Thr595=
ENST00000372220.4:c.810C>A	ENSP00000361294.4:p.Thr270=
ENST00000372228.7:c.2013C>A	ENSP00000361302.3:p.Thr671=
ENST00000402686.7:c.1947C>A	ENSP00000385797.3:p.Thr649=
ENST00000404875.6:c.1596C>A	ENSP00000384531.2:p.Thr532=
ENST00000423007.5:c.1947C>A	ENSP00000404119.1:p.Thr649=
ENST00000485278.5:n.2497C>A
ENST00000494883.1:n.490C>A
NM_001077365.1:c.1947C>A	NP_001070833.1:p.Thr649=
NM_001077366.1:c.1785C>A	NP_001070834.1:p.Thr595=
NM_001136113.1:c.1947C>A	NP_001129585.1:p.Thr649=
NM_001136114.1:c.1596C>A	NP_001129586.1:p.Thr532=
NM_007171.3:c.2013C>A	NP_009102.3:p.Thr671=
XM_005272156.1:c.2013C>A	XP_005272213.1:p.Thr671=
XM_005272158.1:c.1851C>A	XP_005272215.1:p.Thr617=
XM_005272159.1:c.1662C>A	XP_005272216.1:p.Thr554=
XM_005272162.1:c.816C>A	XP_005272219.1:p.Thr272=
XM_006716932.1:c.1662C>A	XP_006716995.1:p.Thr554=
XM_011518140.1:c.1866C>A	XP_011516442.1:p.Thr622=
XM_011518141.1:c.1800C>A	XP_011516443.1:p.Thr600=
XM_011518142.1:c.1704C>A	XP_011516444.1:p.Thr568=
XM_011518143.1:c.1698C>A	XP_011516445.1:p.Thr566=
XM_011518145.1:c.1557C>A	XP_011516447.1:p.Thr519=
XM_011518147.1:c.885C>A	XP_011516449.1:p.Thr295=
XR_929703.1:n.2189C>A
NM_001353193.1:c.2013C>A	NP_001340122.1:p.Thr671=
NM_001353194.1:c.1785C>A	NP_001340123.1:p.Thr595=
NM_001353195.1:c.1596C>A	NP_001340124.1:p.Thr532=
NM_001353196.1:c.1857C>A	NP_001340125.1:p.Thr619=
NM_001353197.1:c.1851C>A	NP_001340126.1:p.Thr617=
NM_001353198.1:c.1851C>A	NP_001340127.1:p.Thr617=
NM_001353199.1:c.1662C>A	NP_001340128.1:p.Thr554=
NM_001353200.1:c.1491C>A	NP_001340129.1:p.Thr497=
NR_148391.1:n.1997C>A
NR_148392.1:n.2215C>A
NR_148393.1:n.2136C>A
NR_148394.1:n.1890C>A
NR_148395.1:n.2288C>A
NR_148396.1:n.1922C>A
NR_148397.1:n.2047C>A
NR_148398.1:n.2002C>A
NR_148399.1:n.2528C>A
NR_148400.1:n.2127C>A
XM_005272162.3:c.816C>A	XP_005272219.1:p.Thr272=
XM_006716932.2:c.1662C>A	XP_006716995.1:p.Thr554=
XM_011518140.2:c.1866C>A	XP_011516442.1:p.Thr622=
XM_011518141.2:c.1800C>A	XP_011516443.1:p.Thr600=
XM_011518142.2:c.1704C>A	XP_011516444.1:p.Thr568=
XM_011518143.2:c.1698C>A	XP_011516445.1:p.Thr566=
XM_011518145.2:c.1557C>A	XP_011516447.1:p.Thr519=
XM_017014205.2:c.816C>A	XP_016869694.1:p.Thr272=
XM_024447380.1:c.816C>A	XP_024303148.1:p.Thr272=
XM_024447381.1:c.1122C>A	XP_024303149.1:p.Thr374=
XM_024447382.1:c.816C>A	XP_024303150.1:p.Thr272=
XR_001746160.2:n.2117C>A
XR_001746162.2:n.2322C>A
XR_001746164.1:n.2039C>A
XR_001746166.2:n.2334C>A
NM_001077365.2:c.1947C>A MANE Select	NP_001070833.1:p.Thr649=
NM_001077366.2:c.1785C>A	NP_001070834.1:p.Thr595=
NM_001136113.2:c.1947C>A	NP_001129585.1:p.Thr649=
NM_001136114.2:c.1596C>A	NP_001129586.1:p.Thr532=
NM_001353193.2:c.2013C>A	NP_001340122.2:p.Thr671=
NM_001353194.2:c.1785C>A	NP_001340123.1:p.Thr595=
NM_001353195.2:c.1596C>A	NP_001340124.1:p.Thr532=
NM_001353196.2:c.1857C>A	NP_001340125.1:p.Thr619=
NM_001353197.2:c.1851C>A	NP_001340126.2:p.Thr617=
NM_001353198.2:c.1851C>A	NP_001340127.2:p.Thr617=
NM_001353199.2:c.1662C>A	NP_001340128.2:p.Thr554=
NM_001353200.2:c.1491C>A	NP_001340129.1:p.Thr497=
NM_001374689.1:c.1935C>A	NP_001361618.1:p.Thr645=
NM_001374690.1:c.1728C>A	NP_001361619.1:p.Thr576=
NM_001374691.1:c.1596C>A	NP_001361620.1:p.Thr532=
NM_001374692.1:c.1596C>A	NP_001361621.1:p.Thr532=
NM_001374693.1:c.1596C>A	NP_001361622.1:p.Thr532=
NM_001374695.1:c.1557C>A	NP_001361624.1:p.Thr519=
NM_007171.4:c.2013C>A	NP_009102.4:p.Thr671=
NR_148391.2:n.1981C>A
NR_148392.2:n.2199C>A
NR_148393.2:n.2120C>A
NR_148394.2:n.1874C>A
NR_148395.2:n.2272C>A
NR_148396.2:n.1906C>A
NR_148397.2:n.2031C>A
NR_148398.2:n.1986C>A
NR_148399.2:n.2512C>A
NR_148400.2:n.2111C>A