Canonical Allele Identifier: CA1468148879

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420284G= , CM000666.2:g.73420284G=	GRCh38
NC_000004.11:g.74286001G= , CM000666.1:g.74286001G=	GRCh37
NC_000004.10:g.74504865G=	NCBI36
NG_009291.1:g.21030G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1816G= MANE Select	ENSP00000295897.4:p.Ala606=
ENST00000295897.8:c.1816G=	ENSP00000295897.4:p.Ala606=
ENST00000401494.7:c.1471G=	ENSP00000384695.3:p.Ala491=
ENST00000415165.6:c.1240G=	ENSP00000401820.2:p.Ala414=
ENST00000476441.6:c.*1095G=	ENSP00000423727.1:n.*1095G=
ENST00000495173.1:n.124G=
ENST00000503124.5:c.1366G=	ENSP00000421027.1:p.Ala456=
ENST00000505649.5:n.1363G=
ENST00000508932.5:n.206G=
ENST00000509063.5:c.1785+645G=	ENSP00000422784.1:n.1785+645G=
ENST00000511370.1:c.1349G=
ENST00000621085.4:c.1177G=	ENSP00000483421.1:p.Ala393=
ENST00000621628.4:c.1177G=	ENSP00000480485.1:p.Ala393=
NM_000477.5:c.1816G=	NP_000468.1:p.Ala606=
NM_000477.6:c.1816G=	NP_000468.1:p.Ala606=
NM_000477.7:c.1816G= MANE Select	NP_000468.1:p.Ala606=