Canonical Allele Identifier: CA1468148560

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404388G= , CM000666.2:g.73404388G=	GRCh38
NC_000004.11:g.74270105G= , CM000666.1:g.74270105G=	GRCh37
NC_000004.10:g.74488969G=	NCBI36
NG_009291.1:g.5134G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.61G= MANE Select	ENSP00000295897.4:p.Val21=
ENST00000295897.8:c.61G=	ENSP00000295897.4:p.Val21=
ENST00000401494.7:c.61G=	ENSP00000384695.3:p.Val21=
ENST00000415165.6:c.61G=	ENSP00000401820.2:p.Val21=
ENST00000441319.5:c.67G=	ENSP00000392541.1:p.Val23=
ENST00000476441.6:c.61G=	ENSP00000423727.1:p.Val21=
ENST00000503124.5:c.-120G=	ENSP00000421027.1:n.-120G=
ENST00000509063.5:c.61G=	ENSP00000422784.1:p.Val21=
ENST00000510166.5:n.102G=
ENST00000514786.1:n.48+52G=
ENST00000515133.5:n.102G=
ENST00000621085.4:c.61G=	ENSP00000483421.1:p.Val21=
ENST00000621628.4:c.61G=	ENSP00000480485.1:p.Val21=
NM_000477.5:c.61G=	NP_000468.1:p.Val21=
NM_000477.6:c.61G=	NP_000468.1:p.Val21=
NM_000477.7:c.61G= MANE Select	NP_000468.1:p.Val21=