Canonical Allele Identifier: CA1468148697

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404435C= , CM000666.2:g.73404435C=	GRCh38
NC_000004.11:g.74270152C= , CM000666.1:g.74270152C=	GRCh37
NC_000004.10:g.74489016C=	NCBI36
NG_009291.1:g.5181C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.79+29C= MANE Select	ENSP00000295897.4:n.79+29C=
ENST00000295897.8:c.79+29C=	ENSP00000295897.4:n.79+29C=
ENST00000401494.7:c.79+29C=	ENSP00000384695.3:n.79+29C=
ENST00000415165.6:c.79+29C=	ENSP00000401820.2:n.79+29C=
ENST00000441319.5:c.85+29C=	ENSP00000392541.1:n.85+29C=
ENST00000476441.6:c.79+29C=	ENSP00000423727.1:n.79+29C=
ENST00000503124.5:c.-102+29C=	ENSP00000421027.1:n.-102+29C=
ENST00000509063.5:c.79+29C=	ENSP00000422784.1:n.79+29C=
ENST00000510166.5:n.120+29C=
ENST00000514786.1:n.48+99C=
ENST00000515133.5:n.120+29C=
ENST00000621085.4:c.79+29C=	ENSP00000483421.1:n.79+29C=
ENST00000621628.4:c.79+29C=	ENSP00000480485.1:n.79+29C=
NM_000477.5:c.79+29C=	NP_000468.1:n.79+29C=
NM_000477.6:c.79+29C=	NP_000468.1:n.79+29C=
NM_000477.7:c.79+29C= MANE Select	NP_000468.1:n.79+29C=