Canonical Allele Identifier: CA1468148628

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404403G= , CM000666.2:g.73404403G=	GRCh38
NC_000004.11:g.74270120G= , CM000666.1:g.74270120G=	GRCh37
NC_000004.10:g.74488984G=	NCBI36
NG_009291.1:g.5149G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.76G= MANE Select	ENSP00000295897.4:p.Ala26=
ENST00000295897.8:c.76G=	ENSP00000295897.4:p.Ala26=
ENST00000401494.7:c.76G=	ENSP00000384695.3:p.Ala26=
ENST00000415165.6:c.76G=	ENSP00000401820.2:p.Ala26=
ENST00000441319.5:c.82G=	ENSP00000392541.1:p.Ala28=
ENST00000476441.6:c.76G=	ENSP00000423727.1:p.Ala26=
ENST00000503124.5:c.-105G=	ENSP00000421027.1:n.-105G=
ENST00000509063.5:c.76G=	ENSP00000422784.1:p.Ala26=
ENST00000510166.5:n.117G=
ENST00000514786.1:n.48+67G=
ENST00000515133.5:n.117G=
ENST00000621085.4:c.76G=	ENSP00000483421.1:p.Ala26=
ENST00000621628.4:c.76G=	ENSP00000480485.1:p.Ala26=
NM_000477.5:c.76G=	NP_000468.1:p.Ala26=
NM_000477.6:c.76G=	NP_000468.1:p.Ala26=
NM_000477.7:c.76G= MANE Select	NP_000468.1:p.Ala26=