Canonical Allele Identifier: CA2003793518

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093257G= , CM000673.2:g.119093257G=	GRCh38
NC_000011.9:g.118963967G= , CM000673.1:g.118963967G=	GRCh37
NC_000011.8:g.118469177G=	NCBI36
NG_008093.1:g.13381G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.895G=	ENSP00000509288.1:p.Ala299=
ENST00000691144.1:n.3275G=
ENST00000691249.1:n.1884G=
ENST00000442944.7:c.1042G=	ENSP00000392041.3:p.Ala348=
ENST00000640813.1:c.*297G=	ENSP00000491061.1:n.*297G=
ENST00000648026.1:c.954G=	ENSP00000498044.1:n.954G=
ENST00000648374.1:c.1009G=	ENSP00000497255.1:p.Ala337=
ENST00000650101.1:c.991G=	ENSP00000496970.1:p.Ala331=
ENST00000650307.1:n.1886G=
ENST00000652429.1:c.1060G= MANE Select	ENSP00000498786.1:p.Ala354=
ENST00000278715.7:c.1060G=	ENSP00000278715.3:p.Ala354=
ENST00000392841.1:c.1009G=	ENSP00000376584.1:p.Ala337=
ENST00000442944.6:c.1009G=	ENSP00000392041.2:p.Ala337=
ENST00000537841.5:c.1009G=	ENSP00000444730.1:p.Ala337=
ENST00000539045.1:n.559G=
ENST00000542044.5:n.1505G=
ENST00000542729.5:c.889G=	ENSP00000443058.1:p.Ala297=
ENST00000543090.5:c.967G=	ENSP00000445429.1:p.Ala323=
ENST00000543543.5:n.1535G=
ENST00000544182.1:n.1509G=
ENST00000544387.5:c.940G=	ENSP00000438424.1:p.Ala314=
ENST00000546226.5:n.1822G=
NM_000190.3:c.1060G=	NP_000181.2:p.Ala354=
NM_001024382.1:c.1009G=	NP_001019553.1:p.Ala337=
NM_001258208.1:c.940G=	NP_001245137.1:p.Ala314=
NM_001258209.1:c.889G=	NP_001245138.1:p.Ala297=
XM_005271531.1:c.1009G=	XP_005271588.1:p.Ala337=
XM_005271532.1:c.1009G=	XP_005271589.1:p.Ala337=
XM_005271533.2:c.1006G=	XP_005271590.1:p.Ala336=
XM_011542796.1:c.895G=	XP_011541098.1:p.Ala299=
NM_000190.4:c.1060G= MANE Select	NP_000181.2:p.Ala354=
NM_001024382.2:c.1009G=	NP_001019553.1:p.Ala337=
XM_005271533.3:c.1006G=	XP_005271590.1:p.Ala336=
XM_017017629.1:c.1009G=	XP_016873118.1:p.Ala337=
XM_024448460.1:c.886G=	XP_024304228.1:p.Ala296=
NM_001258208.2:c.940G=	NP_001245137.1:p.Ala314=
NM_001258209.2:c.889G=	NP_001245138.1:p.Ala297=