Canonical Allele Identifier: CA382900043

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963965T>A (hg19) ; chr11:g.119093255T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093255T>A , CM000673.2:g.119093255T>A	GRCh38
NC_000011.9:g.118963965T>A , CM000673.1:g.118963965T>A	GRCh37
NC_000011.8:g.118469175T>A	NCBI36
NG_008093.1:g.13379T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.893T>A	ENSP00000509288.1:p.Val298Asp
ENST00000691144.1:n.3273T>A
ENST00000691249.1:n.1882T>A
ENST00000442944.7:c.1040T>A	ENSP00000392041.3:p.Val347Asp
ENST00000640813.1:c.*295T>A	ENSP00000491061.1:n.*295T>A
ENST00000648026.1:c.952T>A	ENSP00000498044.1:n.952T>A
ENST00000648374.1:c.1007T>A	ENSP00000497255.1:p.Val336Asp
ENST00000650101.1:c.989T>A	ENSP00000496970.1:p.Val330Asp
ENST00000650307.1:n.1884T>A
ENST00000652429.1:c.1058T>A MANE Select	ENSP00000498786.1:p.Val353Asp
ENST00000278715.7:c.1058T>A	ENSP00000278715.3:p.Val353Asp
ENST00000392841.1:c.1007T>A	ENSP00000376584.1:p.Val336Asp
ENST00000442944.6:c.1007T>A	ENSP00000392041.2:p.Val336Asp
ENST00000537841.5:c.1007T>A	ENSP00000444730.1:p.Val336Asp
ENST00000539045.1:n.557T>A
ENST00000542044.5:n.1503T>A
ENST00000542729.5:c.887T>A	ENSP00000443058.1:p.Val296Asp
ENST00000543090.5:c.965T>A	ENSP00000445429.1:p.Val322Asp
ENST00000543543.5:n.1533T>A
ENST00000544182.1:n.1507T>A
ENST00000544387.5:c.938T>A	ENSP00000438424.1:p.Val313Asp
ENST00000546226.5:n.1820T>A
NM_000190.3:c.1058T>A	NP_000181.2:p.Val353Asp
NM_001024382.1:c.1007T>A	NP_001019553.1:p.Val336Asp
NM_001258208.1:c.938T>A	NP_001245137.1:p.Val313Asp
NM_001258209.1:c.887T>A	NP_001245138.1:p.Val296Asp
XM_005271531.1:c.1007T>A	XP_005271588.1:p.Val336Asp
XM_005271532.1:c.1007T>A	XP_005271589.1:p.Val336Asp
XM_005271533.2:c.1004T>A	XP_005271590.1:p.Val335Asp
XM_011542796.1:c.893T>A	XP_011541098.1:p.Val298Asp
NM_000190.4:c.1058T>A MANE Select	NP_000181.2:p.Val353Asp
NM_001024382.2:c.1007T>A	NP_001019553.1:p.Val336Asp
XM_005271533.3:c.1004T>A	XP_005271590.1:p.Val335Asp
XM_017017629.1:c.1007T>A	XP_016873118.1:p.Val336Asp
XM_024448460.1:c.884T>A	XP_024304228.1:p.Val295Asp
NM_001258208.2:c.938T>A	NP_001245137.1:p.Val313Asp
NM_001258209.2:c.887T>A	NP_001245138.1:p.Val296Asp