Canonical Allele Identifier: CA2003793290

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093146G= , CM000673.2:g.119093146G=	GRCh38
NC_000011.9:g.118963856G= , CM000673.1:g.118963856G=	GRCh37
NC_000011.8:g.118469066G=	NCBI36
NG_008093.1:g.13270G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.784G=	ENSP00000509288.1:p.Gly262=
ENST00000691144.1:n.3164G=
ENST00000691249.1:n.1773G=
ENST00000442944.7:c.931G=	ENSP00000392041.3:p.Gly311=
ENST00000640813.1:c.*186G=	ENSP00000491061.1:n.*186G=
ENST00000648026.1:c.843G=	ENSP00000498044.1:n.843G=
ENST00000648374.1:c.898G=	ENSP00000497255.1:p.Gly300=
ENST00000650101.1:c.880G=	ENSP00000496970.1:p.Gly294=
ENST00000650307.1:n.1775G=
ENST00000652429.1:c.949G= MANE Select	ENSP00000498786.1:p.Gly317=
ENST00000278715.7:c.949G=	ENSP00000278715.3:p.Gly317=
ENST00000392841.1:c.898G=	ENSP00000376584.1:p.Gly300=
ENST00000442944.6:c.898G=	ENSP00000392041.2:p.Gly300=
ENST00000537841.5:c.898G=	ENSP00000444730.1:p.Gly300=
ENST00000539045.1:n.448G=
ENST00000542044.5:n.1394G=
ENST00000542729.5:c.778G=	ENSP00000443058.1:p.Gly260=
ENST00000543090.5:c.856G=	ENSP00000445429.1:p.Gly286=
ENST00000543543.5:n.1424G=
ENST00000544182.1:n.1398G=
ENST00000544387.5:c.829G=	ENSP00000438424.1:p.Gly277=
ENST00000546226.5:n.1711G=
NM_000190.3:c.949G=	NP_000181.2:p.Gly317=
NM_001024382.1:c.898G=	NP_001019553.1:p.Gly300=
NM_001258208.1:c.829G=	NP_001245137.1:p.Gly277=
NM_001258209.1:c.778G=	NP_001245138.1:p.Gly260=
XM_005271531.1:c.898G=	XP_005271588.1:p.Gly300=
XM_005271532.1:c.898G=	XP_005271589.1:p.Gly300=
XM_005271533.2:c.895G=	XP_005271590.1:p.Gly299=
XM_011542796.1:c.784G=	XP_011541098.1:p.Gly262=
NM_000190.4:c.949G= MANE Select	NP_000181.2:p.Gly317=
NM_001024382.2:c.898G=	NP_001019553.1:p.Gly300=
XM_005271533.3:c.895G=	XP_005271590.1:p.Gly299=
XM_017017629.1:c.898G=	XP_016873118.1:p.Gly300=
XM_024448460.1:c.775G=	XP_024304228.1:p.Gly259=
NM_001258208.2:c.829G=	NP_001245137.1:p.Gly277=
NM_001258209.2:c.778G=	NP_001245138.1:p.Gly260=