Canonical Allele Identifier: CA1468144743

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73416262G= , CM000666.2:g.73416262G=	GRCh38
NC_000004.11:g.74281979G= , CM000666.1:g.74281979G=	GRCh37
NC_000004.10:g.74500843G=	NCBI36
NG_009291.1:g.17008G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1198G= MANE Select	ENSP00000295897.4:p.Glu400=
ENST00000295897.8:c.1198G=	ENSP00000295897.4:p.Glu400=
ENST00000401494.7:c.853G=	ENSP00000384695.3:p.Glu285=
ENST00000415165.6:c.622G=	ENSP00000401820.2:p.Glu208=
ENST00000476441.6:c.*477G=	ENSP00000423727.1:n.*477G=
ENST00000484992.1:n.518G=
ENST00000503124.5:c.748G=	ENSP00000421027.1:p.Glu250=
ENST00000505649.5:n.884G=
ENST00000509063.5:c.1198G=	ENSP00000422784.1:p.Glu400=
ENST00000511370.1:c.731G=
ENST00000621085.4:c.559G=	ENSP00000483421.1:p.Glu187=
ENST00000621628.4:c.559G=	ENSP00000480485.1:p.Glu187=
NM_000477.5:c.1198G=	NP_000468.1:p.Glu400=
NM_000477.6:c.1198G=	NP_000468.1:p.Glu400=
NM_000477.7:c.1198G= MANE Select	NP_000468.1:p.Glu400=