Canonical Allele Identifier: CA1468146924

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418232G= , CM000666.2:g.73418232G=	GRCh38
NC_000004.11:g.74283949G= , CM000666.1:g.74283949G=	GRCh37
NC_000004.10:g.74502813G=	NCBI36
NG_009291.1:g.18978G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1573G= MANE Select	ENSP00000295897.4:p.Glu525=
ENST00000295897.8:c.1573G=	ENSP00000295897.4:p.Glu525=
ENST00000401494.7:c.1228G=	ENSP00000384695.3:p.Glu410=
ENST00000415165.6:c.997G=	ENSP00000401820.2:p.Glu333=
ENST00000476441.6:c.*852G=	ENSP00000423727.1:n.*852G=
ENST00000486939.1:n.227G=
ENST00000503124.5:c.1123G=	ENSP00000421027.1:p.Glu375=
ENST00000505649.5:n.1120G=
ENST00000509063.5:c.1573G=	ENSP00000422784.1:p.Glu525=
ENST00000511370.1:c.1106G=
ENST00000621085.4:c.934G=	ENSP00000483421.1:p.Glu312=
ENST00000621628.4:c.934G=	ENSP00000480485.1:p.Glu312=
NM_000477.5:c.1573G=	NP_000468.1:p.Glu525=
NM_000477.6:c.1573G=	NP_000468.1:p.Glu525=
NM_000477.7:c.1573G= MANE Select	NP_000468.1:p.Glu525=