Canonical Allele Identifier: CA382897188

Gene: HMBS

Linked Data

• MyVariant Identifiers: chr11:g.118963132G>A (hg19) ; chr11:g.119092422G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092422G>A , CM000673.2:g.119092422G>A	GRCh38
NC_000011.9:g.118963132G>A , CM000673.1:g.118963132G>A	GRCh37
NC_000011.8:g.118468342G>A	NCBI36
NG_008093.1:g.12546G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000686218.1:c.505G>A	ENSP00000509288.1:p.Val169Met
ENST00000691144.1:n.2651G>A
ENST00000691249.1:n.1494G>A
ENST00000442944.7:c.652G>A	ENSP00000392041.3:p.Val218Met
ENST00000536813.6:c.619G>A	ENSP00000438726.2:p.Val207Met
ENST00000640813.1:c.480G>A	ENSP00000491061.1:p.Lys160=
ENST00000648026.1:c.564G>A	ENSP00000498044.1:p.Lys188=
ENST00000648374.1:c.619G>A	ENSP00000497255.1:p.Val207Met
ENST00000649823.1:n.1127G>A
ENST00000650101.1:c.601G>A	ENSP00000496970.1:p.Val201Met
ENST00000650307.1:n.1496G>A
ENST00000652429.1:c.670G>A MANE Select	ENSP00000498786.1:p.Val224Met
ENST00000278715.7:c.670G>A	ENSP00000278715.3:p.Val224Met
ENST00000392841.1:c.619G>A	ENSP00000376584.1:p.Val207Met
ENST00000442944.6:c.619G>A	ENSP00000392041.2:p.Val207Met
ENST00000537841.5:c.619G>A	ENSP00000444730.1:p.Val207Met
ENST00000542044.5:n.1115G>A
ENST00000542729.5:c.600+259G>A	ENSP00000443058.1:n.600+259G>A
ENST00000543090.5:c.577G>A	ENSP00000445429.1:p.Val193Met
ENST00000543543.5:n.1145G>A
ENST00000544182.1:n.885G>A
ENST00000544387.5:c.651+259G>A	ENSP00000438424.1:n.651+259G>A
ENST00000545621.5:c.*805G>A	ENSP00000444849.1:n.*805G>A
ENST00000546226.5:n.1198G>A
NM_000190.3:c.670G>A	NP_000181.2:p.Val224Met
NM_001024382.1:c.619G>A	NP_001019553.1:p.Val207Met
NM_001258208.1:c.651+259G>A	NP_001245137.1:n.651+259G>A
NM_001258209.1:c.600+259G>A	NP_001245138.1:n.600+259G>A
XM_005271531.1:c.619G>A	XP_005271588.1:p.Val207Met
XM_005271532.1:c.619G>A	XP_005271589.1:p.Val207Met
XM_005271533.2:c.616G>A	XP_005271590.1:p.Val206Met
XM_011542796.1:c.505G>A	XP_011541098.1:p.Val169Met
NM_000190.4:c.670G>A MANE Select	NP_000181.2:p.Val224Met
NM_001024382.2:c.619G>A	NP_001019553.1:p.Val207Met
XM_005271533.3:c.616G>A	XP_005271590.1:p.Val206Met
XM_017017629.1:c.619G>A	XP_016873118.1:p.Val207Met
XM_024448460.1:c.597+259G>A	XP_024304228.1:n.597+259G>A
NM_001258208.2:c.651+259G>A	NP_001245137.1:n.651+259G>A
NM_001258209.2:c.600+259G>A	NP_001245138.1:n.600+259G>A