Canonical Allele Identifier: CA382899145

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963839A>T (hg19) ; chr11:g.119093129A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093129A>T , CM000673.2:g.119093129A>T	GRCh38
NC_000011.9:g.118963839A>T , CM000673.1:g.118963839A>T	GRCh37
NC_000011.8:g.118469049A>T	NCBI36
NG_008093.1:g.13253A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.767A>T	ENSP00000509288.1:p.Asp256Val
ENST00000691144.1:n.3147A>T
ENST00000691249.1:n.1756A>T
ENST00000442944.7:c.914A>T	ENSP00000392041.3:p.Asp305Val
ENST00000640813.1:c.*169A>T	ENSP00000491061.1:n.*169A>T
ENST00000648026.1:c.826A>T	ENSP00000498044.1:n.826A>T
ENST00000648374.1:c.881A>T	ENSP00000497255.1:p.Asp294Val
ENST00000650101.1:c.863A>T	ENSP00000496970.1:p.Asp288Val
ENST00000650307.1:n.1758A>T
ENST00000652429.1:c.932A>T MANE Select	ENSP00000498786.1:p.Asp311Val
ENST00000278715.7:c.932A>T	ENSP00000278715.3:p.Asp311Val
ENST00000392841.1:c.881A>T	ENSP00000376584.1:p.Asp294Val
ENST00000442944.6:c.881A>T	ENSP00000392041.2:p.Asp294Val
ENST00000537841.5:c.881A>T	ENSP00000444730.1:p.Asp294Val
ENST00000539045.1:n.431A>T
ENST00000542044.5:n.1377A>T
ENST00000542729.5:c.761A>T	ENSP00000443058.1:p.Asp254Val
ENST00000543090.5:c.839A>T	ENSP00000445429.1:p.Asp280Val
ENST00000543543.5:n.1407A>T
ENST00000544182.1:n.1381A>T
ENST00000544387.5:c.812A>T	ENSP00000438424.1:p.Asp271Val
ENST00000546226.5:n.1694A>T
NM_000190.3:c.932A>T	NP_000181.2:p.Asp311Val
NM_001024382.1:c.881A>T	NP_001019553.1:p.Asp294Val
NM_001258208.1:c.812A>T	NP_001245137.1:p.Asp271Val
NM_001258209.1:c.761A>T	NP_001245138.1:p.Asp254Val
XM_005271531.1:c.881A>T	XP_005271588.1:p.Asp294Val
XM_005271532.1:c.881A>T	XP_005271589.1:p.Asp294Val
XM_005271533.2:c.878A>T	XP_005271590.1:p.Asp293Val
XM_011542796.1:c.767A>T	XP_011541098.1:p.Asp256Val
NM_000190.4:c.932A>T MANE Select	NP_000181.2:p.Asp311Val
NM_001024382.2:c.881A>T	NP_001019553.1:p.Asp294Val
XM_005271533.3:c.878A>T	XP_005271590.1:p.Asp293Val
XM_017017629.1:c.881A>T	XP_016873118.1:p.Asp294Val
XM_024448460.1:c.758A>T	XP_024304228.1:p.Asp253Val
NM_001258208.2:c.812A>T	NP_001245137.1:p.Asp271Val
NM_001258209.2:c.761A>T	NP_001245138.1:p.Asp254Val