Canonical Allele Identifier: CA2003793480

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119093240A= , CM000673.2:g.119093240A=	GRCh38
NC_000011.9:g.118963950A= , CM000673.1:g.118963950A=	GRCh37
NC_000011.8:g.118469160A=	NCBI36
NG_008093.1:g.13364A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.878A=	ENSP00000509288.1:p.Lys293=
ENST00000691144.1:n.3258A=
ENST00000691249.1:n.1867A=
ENST00000442944.7:c.1025A=	ENSP00000392041.3:p.Lys342=
ENST00000640813.1:c.*280A=	ENSP00000491061.1:n.*280A=
ENST00000648026.1:c.937A=	ENSP00000498044.1:n.937A=
ENST00000648374.1:c.992A=	ENSP00000497255.1:p.Lys331=
ENST00000650101.1:c.974A=	ENSP00000496970.1:p.Lys325=
ENST00000650307.1:n.1869A=
ENST00000652429.1:c.1043A= MANE Select	ENSP00000498786.1:p.Lys348=
ENST00000278715.7:c.1043A=	ENSP00000278715.3:p.Lys348=
ENST00000392841.1:c.992A=	ENSP00000376584.1:p.Lys331=
ENST00000442944.6:c.992A=	ENSP00000392041.2:p.Lys331=
ENST00000537841.5:c.992A=	ENSP00000444730.1:p.Lys331=
ENST00000539045.1:n.542A=
ENST00000542044.5:n.1488A=
ENST00000542729.5:c.872A=	ENSP00000443058.1:p.Lys291=
ENST00000543090.5:c.950A=	ENSP00000445429.1:p.Lys317=
ENST00000543543.5:n.1518A=
ENST00000544182.1:n.1492A=
ENST00000544387.5:c.923A=	ENSP00000438424.1:p.Lys308=
ENST00000546226.5:n.1805A=
NM_000190.3:c.1043A=	NP_000181.2:p.Lys348=
NM_001024382.1:c.992A=	NP_001019553.1:p.Lys331=
NM_001258208.1:c.923A=	NP_001245137.1:p.Lys308=
NM_001258209.1:c.872A=	NP_001245138.1:p.Lys291=
XM_005271531.1:c.992A=	XP_005271588.1:p.Lys331=
XM_005271532.1:c.992A=	XP_005271589.1:p.Lys331=
XM_005271533.2:c.989A=	XP_005271590.1:p.Lys330=
XM_011542796.1:c.878A=	XP_011541098.1:p.Lys293=
NM_000190.4:c.1043A= MANE Select	NP_000181.2:p.Lys348=
NM_001024382.2:c.992A=	NP_001019553.1:p.Lys331=
XM_005271533.3:c.989A=	XP_005271590.1:p.Lys330=
XM_017017629.1:c.992A=	XP_016873118.1:p.Lys331=
XM_024448460.1:c.869A=	XP_024304228.1:p.Lys290=
NM_001258208.2:c.923A=	NP_001245137.1:p.Lys308=
NM_001258209.2:c.872A=	NP_001245138.1:p.Lys291=