Canonical Allele Identifier: CA1468150497

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406256C= , CM000666.2:g.73406256C=	GRCh38
NC_000004.11:g.74271973C= , CM000666.1:g.74271973C=	GRCh37
NC_000004.10:g.74490837C=	NCBI36
NG_009291.1:g.7002C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.138-373C= MANE Select	ENSP00000295897.4:n.138-373C=
ENST00000295897.8:c.138-373C=	ENSP00000295897.4:n.138-373C=
ENST00000401494.7:c.137+1083C=	ENSP00000384695.3:n.137+1083C=
ENST00000415165.6:c.137+1083C=	ENSP00000401820.2:n.137+1083C=
ENST00000441319.5:c.144-373C=	ENSP00000392541.1:n.144-373C=
ENST00000476441.6:c.79+1850C=	ENSP00000423727.1:n.79+1850C=
ENST00000503124.5:c.-101-373C=	ENSP00000421027.1:n.-101-373C=
ENST00000509063.5:c.138-373C=	ENSP00000422784.1:n.138-373C=
ENST00000510166.5:n.174-373C=
ENST00000514786.1:n.107-373C=
ENST00000515133.5:n.179-373C=
ENST00000621085.4:c.138-373C=	ENSP00000483421.1:n.138-373C=
ENST00000621628.4:c.138-373C=	ENSP00000480485.1:n.138-373C=
NM_000477.5:c.138-373C=	NP_000468.1:n.138-373C=
NM_000477.6:c.138-373C=	NP_000468.1:n.138-373C=
NM_000477.7:c.138-373C= MANE Select	NP_000468.1:n.138-373C=