Canonical Allele Identifier: CA1468148286

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419604A= , CM000666.2:g.73419604A=	GRCh38
NC_000004.11:g.74285321A= , CM000666.1:g.74285321A=	GRCh37
NC_000004.10:g.74504185A=	NCBI36
NG_009291.1:g.20350A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1750A= MANE Select	ENSP00000295897.4:p.Lys584=
ENST00000295897.8:c.1750A=	ENSP00000295897.4:p.Lys584=
ENST00000401494.7:c.1405A=	ENSP00000384695.3:p.Lys469=
ENST00000415165.6:c.1174A=	ENSP00000401820.2:p.Lys392=
ENST00000476441.6:c.*1029A=	ENSP00000423727.1:n.*1029A=
ENST00000495173.1:n.58A=
ENST00000503124.5:c.1300A=	ENSP00000421027.1:p.Lys434=
ENST00000505649.5:n.1297A=
ENST00000508932.5:n.175+149A=
ENST00000509063.5:c.1750A=	ENSP00000422784.1:p.Lys584=
ENST00000511370.1:c.1283A=
ENST00000621085.4:c.1111A=	ENSP00000483421.1:p.Lys371=
ENST00000621628.4:c.1111A=	ENSP00000480485.1:p.Lys371=
NM_000477.5:c.1750A=	NP_000468.1:p.Lys584=
NM_000477.6:c.1750A=	NP_000468.1:p.Lys584=
NM_000477.7:c.1750A= MANE Select	NP_000468.1:p.Lys584=