Canonical Allele Identifier: CA1468152682

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409397C= , CM000666.2:g.73409397C=	GRCh38
NC_000004.11:g.74275114C= , CM000666.1:g.74275114C=	GRCh37
NC_000004.10:g.74493978C=	NCBI36
NG_009291.1:g.10143C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.525C= MANE Select	ENSP00000295897.4:p.Ala175=
ENST00000295897.8:c.525C=	ENSP00000295897.4:p.Ala175=
ENST00000401494.7:c.180C=	ENSP00000384695.3:p.Ala60=
ENST00000415165.6:c.138-2599C=	ENSP00000401820.2:n.138-2599C=
ENST00000441319.5:c.531C=	ENSP00000392541.1:p.Ala177=
ENST00000476441.6:c.122C=	ENSP00000423727.1:p.Pro41=
ENST00000503124.5:c.75C=	ENSP00000421027.1:p.Ala25=
ENST00000505649.5:n.211C=
ENST00000509063.5:c.525C=	ENSP00000422784.1:p.Ala175=
ENST00000511370.1:c.58C=
ENST00000514786.1:n.494C=
ENST00000621085.4:c.490+35C=	ENSP00000483421.1:n.490+35C=
ENST00000621628.4:c.486+321C=	ENSP00000480485.1:n.486+321C=
NM_000477.5:c.525C=	NP_000468.1:p.Ala175=
NM_000477.6:c.525C=	NP_000468.1:p.Ala175=
NM_000477.7:c.525C= MANE Select	NP_000468.1:p.Ala175=