Canonical Allele Identifier: CA2003792753

Gene: HMBS

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.119092963T= , CM000673.2:g.119092963T=	GRCh38
NC_000011.9:g.118963673T= , CM000673.1:g.118963673T=	GRCh37
NC_000011.8:g.118468883T=	NCBI36
NG_008093.1:g.13087T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000686218.1:c.689T=	ENSP00000509288.1:p.Leu230=
ENST00000691144.1:n.3069T=
ENST00000691249.1:n.1678T=
ENST00000442944.7:c.836T=	ENSP00000392041.3:p.Leu279=
ENST00000640813.1:c.*91T=	ENSP00000491061.1:n.*91T=
ENST00000648026.1:c.748T=	ENSP00000498044.1:n.748T=
ENST00000648374.1:c.803T=	ENSP00000497255.1:p.Leu268=
ENST00000650101.1:c.785T=	ENSP00000496970.1:p.Leu262=
ENST00000650307.1:n.1680T=
ENST00000652429.1:c.854T= MANE Select	ENSP00000498786.1:p.Leu285=
ENST00000278715.7:c.854T=	ENSP00000278715.3:p.Leu285=
ENST00000392841.1:c.803T=	ENSP00000376584.1:p.Leu268=
ENST00000442944.6:c.803T=	ENSP00000392041.2:p.Leu268=
ENST00000537841.5:c.803T=	ENSP00000444730.1:p.Leu268=
ENST00000539045.1:n.353T=
ENST00000542044.5:n.1299T=
ENST00000542729.5:c.683T=	ENSP00000443058.1:p.Leu228=
ENST00000543090.5:c.761T=	ENSP00000445429.1:p.Leu254=
ENST00000543543.5:n.1329T=
ENST00000544182.1:n.1303T=
ENST00000544387.5:c.734T=	ENSP00000438424.1:p.Leu245=
ENST00000546226.5:n.1616T=
NM_000190.3:c.854T=	NP_000181.2:p.Leu285=
NM_001024382.1:c.803T=	NP_001019553.1:p.Leu268=
NM_001258208.1:c.734T=	NP_001245137.1:p.Leu245=
NM_001258209.1:c.683T=	NP_001245138.1:p.Leu228=
XM_005271531.1:c.803T=	XP_005271588.1:p.Leu268=
XM_005271532.1:c.803T=	XP_005271589.1:p.Leu268=
XM_005271533.2:c.800T=	XP_005271590.1:p.Leu267=
XM_011542796.1:c.689T=	XP_011541098.1:p.Leu230=
NM_000190.4:c.854T= MANE Select	NP_000181.2:p.Leu285=
NM_001024382.2:c.803T=	NP_001019553.1:p.Leu268=
XM_005271533.3:c.800T=	XP_005271590.1:p.Leu267=
XM_017017629.1:c.803T=	XP_016873118.1:p.Leu268=
XM_024448460.1:c.680T=	XP_024304228.1:p.Leu227=
NM_001258208.2:c.734T=	NP_001245137.1:p.Leu245=
NM_001258209.2:c.683T=	NP_001245138.1:p.Leu228=