Canonical Allele Identifier: CA2003793416

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093193G= , CM000673.2:g.119093193G=	GRCh38
NC_000011.9:g.118963903G= , CM000673.1:g.118963903G=	GRCh37
NC_000011.8:g.118469113G=	NCBI36
NG_008093.1:g.13317G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.831G=	ENSP00000509288.1:p.Gln277=
ENST00000691144.1:n.3211G=
ENST00000691249.1:n.1820G=
ENST00000442944.7:c.978G=	ENSP00000392041.3:p.Gln326=
ENST00000640813.1:c.*233G=	ENSP00000491061.1:n.*233G=
ENST00000648026.1:c.890G=	ENSP00000498044.1:n.890G=
ENST00000648374.1:c.945G=	ENSP00000497255.1:p.Gln315=
ENST00000650101.1:c.927G=	ENSP00000496970.1:p.Gln309=
ENST00000650307.1:n.1822G=
ENST00000652429.1:c.996G= MANE Select	ENSP00000498786.1:p.Gln332=
ENST00000278715.7:c.996G=	ENSP00000278715.3:p.Gln332=
ENST00000392841.1:c.945G=	ENSP00000376584.1:p.Gln315=
ENST00000442944.6:c.945G=	ENSP00000392041.2:p.Gln315=
ENST00000537841.5:c.945G=	ENSP00000444730.1:p.Gln315=
ENST00000539045.1:n.495G=
ENST00000542044.5:n.1441G=
ENST00000542729.5:c.825G=	ENSP00000443058.1:p.Gln275=
ENST00000543090.5:c.903G=	ENSP00000445429.1:p.Gln301=
ENST00000543543.5:n.1471G=
ENST00000544182.1:n.1445G=
ENST00000544387.5:c.876G=	ENSP00000438424.1:p.Gln292=
ENST00000546226.5:n.1758G=
NM_000190.3:c.996G=	NP_000181.2:p.Gln332=
NM_001024382.1:c.945G=	NP_001019553.1:p.Gln315=
NM_001258208.1:c.876G=	NP_001245137.1:p.Gln292=
NM_001258209.1:c.825G=	NP_001245138.1:p.Gln275=
XM_005271531.1:c.945G=	XP_005271588.1:p.Gln315=
XM_005271532.1:c.945G=	XP_005271589.1:p.Gln315=
XM_005271533.2:c.942G=	XP_005271590.1:p.Gln314=
XM_011542796.1:c.831G=	XP_011541098.1:p.Gln277=
NM_000190.4:c.996G= MANE Select	NP_000181.2:p.Gln332=
NM_001024382.2:c.945G=	NP_001019553.1:p.Gln315=
XM_005271533.3:c.942G=	XP_005271590.1:p.Gln314=
XM_017017629.1:c.945G=	XP_016873118.1:p.Gln315=
XM_024448460.1:c.822G=	XP_024304228.1:p.Gln274=
NM_001258208.2:c.876G=	NP_001245137.1:p.Gln292=
NM_001258209.2:c.825G=	NP_001245138.1:p.Gln275=