Canonical Allele Identifier: CA1468148306

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419613G= , CM000666.2:g.73419613G=	GRCh38
NC_000004.11:g.74285330G= , CM000666.1:g.74285330G=	GRCh37
NC_000004.10:g.74504194G=	NCBI36
NG_009291.1:g.20359G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1759G= MANE Select	NP_000468.1:p.Asp587=
ENST00000295897.9:c.1759G= MANE Select	ENSP00000295897.4:p.Asp587=
NM_000477.5:c.1759G=	NP_000468.1:p.Asp587=
NM_000477.6:c.1759G=	NP_000468.1:p.Asp587=
ENST00000295897.8:c.1759G=	ENSP00000295897.4:p.Asp587=
ENST00000401494.7:c.1414G=	ENSP00000384695.3:p.Asp472=
ENST00000415165.6:c.1183G=	ENSP00000401820.2:p.Asp395=
ENST00000476441.6:c.*1038G=	ENSP00000423727.1:n.*1038G=
ENST00000495173.1:n.67G=
ENST00000503124.5:c.1309G=	ENSP00000421027.1:p.Asp437=
ENST00000505649.5:n.1306G=
ENST00000508932.5:n.175+158G=
ENST00000509063.5:c.1759G=	ENSP00000422784.1:p.Asp587=
ENST00000511370.1:c.1292G=
ENST00000621085.4:c.1120G=	ENSP00000483421.1:p.Asp374=
ENST00000621628.4:c.1120G=	ENSP00000480485.1:p.Asp374=