Canonical Allele Identifier: CA1468148274

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419589G= , CM000666.2:g.73419589G=	GRCh38
NC_000004.11:g.74285306G= , CM000666.1:g.74285306G=	GRCh37
NC_000004.10:g.74504170G=	NCBI36
NG_009291.1:g.20335G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1735G= MANE Select	ENSP00000295897.4:p.Val579=
ENST00000295897.8:c.1735G=	ENSP00000295897.4:p.Val579=
ENST00000401494.7:c.1390G=	ENSP00000384695.3:p.Val464=
ENST00000415165.6:c.1159G=	ENSP00000401820.2:p.Val387=
ENST00000476441.6:c.*1014G=	ENSP00000423727.1:n.*1014G=
ENST00000495173.1:n.43G=
ENST00000503124.5:c.1285G=	ENSP00000421027.1:p.Val429=
ENST00000505649.5:n.1282G=
ENST00000508932.5:n.175+134G=
ENST00000509063.5:c.1735G=	ENSP00000422784.1:p.Val579=
ENST00000511370.1:c.1268G=
ENST00000621085.4:c.1096G=	ENSP00000483421.1:p.Val366=
ENST00000621628.4:c.1096G=	ENSP00000480485.1:p.Val366=
NM_000477.5:c.1735G=	NP_000468.1:p.Val579=
NM_000477.6:c.1735G=	NP_000468.1:p.Val579=
NM_000477.7:c.1735G= MANE Select	NP_000468.1:p.Val579=