Canonical Allele Identifier: CA1468150853

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406640C= , CM000666.2:g.73406640C=	GRCh38
NC_000004.11:g.74272357C= , CM000666.1:g.74272357C=	GRCh37
NC_000004.10:g.74491221C=	NCBI36
NG_009291.1:g.7386C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.149C= MANE Select	ENSP00000295897.4:p.Ala50=
ENST00000295897.8:c.149C=	ENSP00000295897.4:p.Ala50=
ENST00000401494.7:c.137+1467C=	ENSP00000384695.3:n.137+1467C=
ENST00000415165.6:c.137+1467C=	ENSP00000401820.2:n.137+1467C=
ENST00000441319.5:c.155C=	ENSP00000392541.1:p.Ala52=
ENST00000476441.6:c.79+2234C=	ENSP00000423727.1:n.79+2234C=
ENST00000503124.5:c.-90C=	ENSP00000421027.1:n.-90C=
ENST00000509063.5:c.149C=	ENSP00000422784.1:p.Ala50=
ENST00000510166.5:n.185C=
ENST00000514786.1:n.118C=
ENST00000515133.5:n.190C=
ENST00000621085.4:c.149C=	ENSP00000483421.1:p.Ala50=
ENST00000621628.4:c.149C=	ENSP00000480485.1:p.Ala50=
NM_000477.5:c.149C=	NP_000468.1:p.Ala50=
NM_000477.6:c.149C=	NP_000468.1:p.Ala50=
NM_000477.7:c.149C= MANE Select	NP_000468.1:p.Ala50=