Canonical Allele Identifier: CA375315062

Gene: POMT1

Linked Data

• MyVariant Identifiers: chr9:g.134398365T>G (hg19) ; chr9:g.131522978T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.131522978T>G , CM000671.2:g.131522978T>G	GRCh38
NC_000009.11:g.134398365T>G , CM000671.1:g.134398365T>G	GRCh37
NC_000009.10:g.133388186T>G	NCBI36
NG_008896.1:g.25077T>G
NG_008896.2:g.25077T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000341012.13:c.1888T>G	ENSP00000343034.7:p.Tyr630Asp
ENST00000404875.7:n.2590T>G
ENST00000423007.6:c.2107T>G	ENSP00000404119.2:p.Tyr703Asp
ENST00000677295.2:c.*2394T>G	ENSP00000504346.2:n.*2394T>G
ENST00000678264.2:c.*2233T>G	ENSP00000503157.2:n.*2233T>G
ENST00000682070.1:n.2360T>G
ENST00000682639.1:c.47T>G
ENST00000682813.1:n.2447T>G
ENST00000683231.1:c.47T>G
ENST00000683392.1:n.4642T>G
ENST00000683712.1:n.2455T>G
ENST00000683900.1:n.3950T>G
ENST00000684062.1:n.2716T>G
ENST00000684399.1:c.47T>G
ENST00000684579.1:n.3896T>G
ENST00000341012.12:c.1888T>G	ENSP00000343034.7:p.Tyr630Asp
ENST00000372220.5:c.919T>G	ENSP00000361294.5:p.Tyr307Asp
ENST00000372228.9:c.2116T>G	ENSP00000361302.3:p.Tyr706Asp
ENST00000402686.8:c.2050T>G MANE Select	ENSP00000385797.4:p.Tyr684Asp
ENST00000676640.1:c.2050T>G	ENSP00000503281.1:p.Tyr684Asp
ENST00000676803.1:c.1111T>G	ENSP00000503093.1:p.Tyr371Asp
ENST00000676835.1:c.*1265T>G	ENSP00000502911.1:n.*1265T>G
ENST00000677029.1:c.1594T>G	ENSP00000502936.1:p.Tyr532Asp
ENST00000677099.1:c.*1760T>G	ENSP00000504553.1:n.*1760T>G
ENST00000677216.1:c.1699T>G	ENSP00000503772.1:p.Tyr567Asp
ENST00000677221.1:n.1075T>G
ENST00000677295.1:c.*1272T>G	ENSP00000504346.1:n.*1272T>G
ENST00000677444.1:c.1995T>G
ENST00000677586.1:n.1417T>G
ENST00000677626.1:c.1699T>G	ENSP00000503552.1:p.Tyr567Asp
ENST00000677853.1:c.*1058T>G	ENSP00000503488.1:n.*1058T>G
ENST00000678264.1:c.*1427T>G	ENSP00000503157.1:n.*1427T>G
ENST00000678303.1:c.1960T>G	ENSP00000503696.1:p.Tyr654Asp
ENST00000678366.1:c.*2299T>G	ENSP00000504353.1:n.*2299T>G
ENST00000678546.1:c.*1995T>G	ENSP00000503062.1:n.*1995T>G
ENST00000678548.1:c.*2189T>G	ENSP00000503934.1:n.*2189T>G
ENST00000678626.1:n.1886T>G
ENST00000678739.1:c.*2216T>G	ENSP00000503806.1:n.*2216T>G
ENST00000678833.1:c.*1802T>G	ENSP00000503893.1:n.*1802T>G
ENST00000679023.1:c.1888T>G	ENSP00000503718.1:p.Tyr630Asp
ENST00000679076.1:c.1669T>G
ENST00000679111.1:c.*806T>G	ENSP00000504257.1:n.*806T>G
ENST00000679189.1:c.1699T>G	ENSP00000503356.1:p.Tyr567Asp
ENST00000341012.11:c.1888T>G	ENSP00000343034.7:p.Tyr630Asp
ENST00000372220.4:c.913T>G	ENSP00000361294.4:p.Tyr305Asp
ENST00000372228.7:c.2116T>G	ENSP00000361302.3:p.Tyr706Asp
ENST00000402686.7:c.2050T>G	ENSP00000385797.3:p.Tyr684Asp
ENST00000404875.6:c.1699T>G	ENSP00000384531.2:p.Tyr567Asp
ENST00000423007.5:c.2050T>G	ENSP00000404119.1:p.Tyr684Asp
ENST00000485278.5:n.2600T>G
NM_001077365.1:c.2050T>G	NP_001070833.1:p.Tyr684Asp
NM_001077366.1:c.1888T>G	NP_001070834.1:p.Tyr630Asp
NM_001136113.1:c.2050T>G	NP_001129585.1:p.Tyr684Asp
NM_001136114.1:c.1699T>G	NP_001129586.1:p.Tyr567Asp
NM_007171.3:c.2116T>G	NP_009102.3:p.Tyr706Asp
XM_005272156.1:c.2116T>G	XP_005272213.1:p.Tyr706Asp
XM_005272158.1:c.1954T>G	XP_005272215.1:p.Tyr652Asp
XM_005272159.1:c.1765T>G	XP_005272216.1:p.Tyr589Asp
XM_005272162.1:c.919T>G	XP_005272219.1:p.Tyr307Asp
XM_006716932.1:c.1765T>G	XP_006716995.1:p.Tyr589Asp
XM_011518140.1:c.1969T>G	XP_011516442.1:p.Tyr657Asp
XM_011518141.1:c.1903T>G	XP_011516443.1:p.Tyr635Asp
XM_011518142.1:c.1807T>G	XP_011516444.1:p.Tyr603Asp
XM_011518143.1:c.1801T>G	XP_011516445.1:p.Tyr601Asp
XM_011518145.1:c.1660T>G	XP_011516447.1:p.Tyr554Asp
XM_011518147.1:c.988T>G	XP_011516449.1:p.Tyr330Asp
XR_929703.1:n.2292T>G
NM_001353193.1:c.2116T>G	NP_001340122.1:p.Tyr706Asp
NM_001353194.1:c.1888T>G	NP_001340123.1:p.Tyr630Asp
NM_001353195.1:c.1699T>G	NP_001340124.1:p.Tyr567Asp
NM_001353196.1:c.1960T>G	NP_001340125.1:p.Tyr654Asp
NM_001353197.1:c.1954T>G	NP_001340126.1:p.Tyr652Asp
NM_001353198.1:c.1954T>G	NP_001340127.1:p.Tyr652Asp
NM_001353199.1:c.1765T>G	NP_001340128.1:p.Tyr589Asp
NM_001353200.1:c.1594T>G	NP_001340129.1:p.Tyr532Asp
NR_148391.1:n.2100T>G
NR_148392.1:n.2318T>G
NR_148393.1:n.2239T>G
NR_148394.1:n.1993T>G
NR_148395.1:n.2391T>G
NR_148396.1:n.2025T>G
NR_148397.1:n.2150T>G
NR_148398.1:n.2105T>G
NR_148399.1:n.2631T>G
NR_148400.1:n.2230T>G
XM_005272162.3:c.919T>G	XP_005272219.1:p.Tyr307Asp
XM_006716932.2:c.1765T>G	XP_006716995.1:p.Tyr589Asp
XM_011518140.2:c.1969T>G	XP_011516442.1:p.Tyr657Asp
XM_011518141.2:c.1903T>G	XP_011516443.1:p.Tyr635Asp
XM_011518142.2:c.1807T>G	XP_011516444.1:p.Tyr603Asp
XM_011518143.2:c.1801T>G	XP_011516445.1:p.Tyr601Asp
XM_011518145.2:c.1660T>G	XP_011516447.1:p.Tyr554Asp
XM_017014205.2:c.919T>G	XP_016869694.1:p.Tyr307Asp
XM_024447380.1:c.919T>G	XP_024303148.1:p.Tyr307Asp
XM_024447381.1:c.1225T>G	XP_024303149.1:p.Tyr409Asp
XM_024447382.1:c.919T>G	XP_024303150.1:p.Tyr307Asp
XR_001746160.2:n.2220T>G
XR_001746162.2:n.2425T>G
XR_001746164.1:n.2142T>G
XR_001746166.2:n.2437T>G
NM_001077365.2:c.2050T>G MANE Select	NP_001070833.1:p.Tyr684Asp
NM_001077366.2:c.1888T>G	NP_001070834.1:p.Tyr630Asp
NM_001136113.2:c.2050T>G	NP_001129585.1:p.Tyr684Asp
NM_001136114.2:c.1699T>G	NP_001129586.1:p.Tyr567Asp
NM_001353193.2:c.2116T>G	NP_001340122.2:p.Tyr706Asp
NM_001353194.2:c.1888T>G	NP_001340123.1:p.Tyr630Asp
NM_001353195.2:c.1699T>G	NP_001340124.1:p.Tyr567Asp
NM_001353196.2:c.1960T>G	NP_001340125.1:p.Tyr654Asp
NM_001353197.2:c.1954T>G	NP_001340126.2:p.Tyr652Asp
NM_001353198.2:c.1954T>G	NP_001340127.2:p.Tyr652Asp
NM_001353199.2:c.1765T>G	NP_001340128.2:p.Tyr589Asp
NM_001353200.2:c.1594T>G	NP_001340129.1:p.Tyr532Asp
NM_001374689.1:c.2038T>G	NP_001361618.1:p.Tyr680Asp
NM_001374690.1:c.1831T>G	NP_001361619.1:p.Tyr611Asp
NM_001374691.1:c.1699T>G	NP_001361620.1:p.Tyr567Asp
NM_001374692.1:c.1699T>G	NP_001361621.1:p.Tyr567Asp
NM_001374693.1:c.1699T>G	NP_001361622.1:p.Tyr567Asp
NM_001374695.1:c.1660T>G	NP_001361624.1:p.Tyr554Asp
NM_007171.4:c.2116T>G	NP_009102.4:p.Tyr706Asp
NR_148391.2:n.2084T>G
NR_148392.2:n.2302T>G
NR_148393.2:n.2223T>G
NR_148394.2:n.1977T>G
NR_148395.2:n.2375T>G
NR_148396.2:n.2009T>G
NR_148397.2:n.2134T>G
NR_148398.2:n.2089T>G
NR_148399.2:n.2615T>G
NR_148400.2:n.2214T>G