Canonical Allele Identifier: CA1468148875

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420282C= , CM000666.2:g.73420282C=	GRCh38
NC_000004.11:g.74285999C= , CM000666.1:g.74285999C=	GRCh37
NC_000004.10:g.74504863C=	NCBI36
NG_009291.1:g.21028C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1814C= MANE Select	ENSP00000295897.4:p.Ala605=
ENST00000295897.8:c.1814C=	ENSP00000295897.4:p.Ala605=
ENST00000401494.7:c.1469C=	ENSP00000384695.3:p.Ala490=
ENST00000415165.6:c.1238C=	ENSP00000401820.2:p.Ala413=
ENST00000476441.6:c.*1093C=	ENSP00000423727.1:n.*1093C=
ENST00000495173.1:n.122C=
ENST00000503124.5:c.1364C=	ENSP00000421027.1:p.Ala455=
ENST00000505649.5:n.1361C=
ENST00000508932.5:n.204C=
ENST00000509063.5:c.1785+643C=	ENSP00000422784.1:n.1785+643C=
ENST00000511370.1:c.1347C=
ENST00000621085.4:c.1175C=	ENSP00000483421.1:p.Ala392=
ENST00000621628.4:c.1175C=	ENSP00000480485.1:p.Ala392=
NM_000477.5:c.1814C=	NP_000468.1:p.Ala605=
NM_000477.6:c.1814C=	NP_000468.1:p.Ala605=
NM_000477.7:c.1814C= MANE Select	NP_000468.1:p.Ala605=