Canonical Allele Identifier: CA2003791647

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092476G= , CM000673.2:g.119092476G=	GRCh38
NC_000011.9:g.118963186G= , CM000673.1:g.118963186G=	GRCh37
NC_000011.8:g.118468396G=	NCBI36
NG_008093.1:g.12600G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.559G=	ENSP00000509288.1:p.Glu187=
ENST00000691144.1:n.2705G=
ENST00000691249.1:n.1548G=
ENST00000442944.7:c.706G=	ENSP00000392041.3:p.Glu236=
ENST00000536813.6:c.673G=	ENSP00000438726.2:p.Glu225=
ENST00000640813.1:c.534G=	ENSP00000491061.1:p.Pro178=
ENST00000648026.1:c.618G=	ENSP00000498044.1:p.Pro206=
ENST00000648374.1:c.673G=	ENSP00000497255.1:p.Glu225=
ENST00000649823.1:n.1181G=
ENST00000650101.1:c.655G=	ENSP00000496970.1:p.Glu219=
ENST00000650307.1:n.1550G=
ENST00000652429.1:c.724G= MANE Select	ENSP00000498786.1:p.Glu242=
ENST00000278715.7:c.724G=	ENSP00000278715.3:p.Glu242=
ENST00000392841.1:c.673G=	ENSP00000376584.1:p.Glu225=
ENST00000442944.6:c.673G=	ENSP00000392041.2:p.Glu225=
ENST00000537841.5:c.673G=	ENSP00000444730.1:p.Glu225=
ENST00000542044.5:n.1169G=
ENST00000542729.5:c.601-282G=	ENSP00000443058.1:n.601-282G=
ENST00000543090.5:c.631G=	ENSP00000445429.1:p.Glu211=
ENST00000543543.5:n.1199G=
ENST00000544182.1:n.939G=
ENST00000544387.5:c.652-282G=	ENSP00000438424.1:n.652-282G=
ENST00000545621.5:c.*859G=	ENSP00000444849.1:n.*859G=
ENST00000546226.5:n.1252G=
NM_000190.3:c.724G=	NP_000181.2:p.Glu242=
NM_001024382.1:c.673G=	NP_001019553.1:p.Glu225=
NM_001258208.1:c.652-282G=	NP_001245137.1:n.652-282G=
NM_001258209.1:c.601-282G=	NP_001245138.1:n.601-282G=
XM_005271531.1:c.673G=	XP_005271588.1:p.Glu225=
XM_005271532.1:c.673G=	XP_005271589.1:p.Glu225=
XM_005271533.2:c.670G=	XP_005271590.1:p.Glu224=
XM_011542796.1:c.559G=	XP_011541098.1:p.Glu187=
NM_000190.4:c.724G= MANE Select	NP_000181.2:p.Glu242=
NM_001024382.2:c.673G=	NP_001019553.1:p.Glu225=
XM_005271533.3:c.670G=	XP_005271590.1:p.Glu224=
XM_017017629.1:c.673G=	XP_016873118.1:p.Glu225=
XM_024448460.1:c.598-282G=	XP_024304228.1:n.598-282G=
NM_001258208.2:c.652-282G=	NP_001245137.1:n.652-282G=
NM_001258209.2:c.601-282G=	NP_001245138.1:n.601-282G=