Canonical Allele Identifier: CA1468140756

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73412084G= , CM000666.2:g.73412084G=	GRCh38
NC_000004.11:g.74277801G= , CM000666.1:g.74277801G=	GRCh37
NC_000004.10:g.74496665G=	NCBI36
NG_009291.1:g.12830G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.802G= MANE Select	NP_000468.1:p.Glu268=
ENST00000295897.9:c.802G= MANE Select	ENSP00000295897.4:p.Glu268=
NM_000477.5:c.802G=	NP_000468.1:p.Glu268=
NM_000477.6:c.802G=	NP_000468.1:p.Glu268=
ENST00000295897.8:c.802G=	ENSP00000295897.4:p.Glu268=
ENST00000401494.7:c.457G=	ENSP00000384695.3:p.Glu153=
ENST00000415165.6:c.226G=	ENSP00000401820.2:p.Glu76=
ENST00000476441.6:c.*81G=	ENSP00000423727.1:n.*81G=
ENST00000503124.5:c.352G=	ENSP00000421027.1:p.Glu118=
ENST00000505649.5:n.488G=
ENST00000507673.1:n.119G=
ENST00000509063.5:c.802G=	ENSP00000422784.1:p.Glu268=
ENST00000511370.1:c.335G=
ENST00000621085.4:c.490+2722G=	ENSP00000483421.1:n.490+2722G=
ENST00000621628.4:c.486+3008G=	ENSP00000480485.1:n.486+3008G=