Canonical Allele Identifier: CA1468150974

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406741G= , CM000666.2:g.73406741G=	GRCh38
NC_000004.11:g.74272458G= , CM000666.1:g.74272458G=	GRCh37
NC_000004.10:g.74491322G=	NCBI36
NG_009291.1:g.7487G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.250G= MANE Select	ENSP00000295897.4:p.Glu84=
ENST00000295897.8:c.250G=	ENSP00000295897.4:p.Glu84=
ENST00000401494.7:c.137+1568G=	ENSP00000384695.3:n.137+1568G=
ENST00000415165.6:c.137+1568G=	ENSP00000401820.2:n.137+1568G=
ENST00000441319.5:c.256G=	ENSP00000392541.1:p.Glu86=
ENST00000476441.6:c.79+2335G=	ENSP00000423727.1:n.79+2335G=
ENST00000503124.5:c.12G=	ENSP00000421027.1:p.Leu4=
ENST00000509063.5:c.250G=	ENSP00000422784.1:p.Glu84=
ENST00000510166.5:n.286G=
ENST00000514786.1:n.219G=
ENST00000515133.5:n.291G=
ENST00000621085.4:c.250G=	ENSP00000483421.1:p.Glu84=
ENST00000621628.4:c.250G=	ENSP00000480485.1:p.Glu84=
NM_000477.5:c.250G=	NP_000468.1:p.Glu84=
NM_000477.6:c.250G=	NP_000468.1:p.Glu84=
NM_000477.7:c.250G= MANE Select	NP_000468.1:p.Glu84=