Canonical Allele Identifier: CA1468148363

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419636G= , CM000666.2:g.73419636G=	GRCh38
NC_000004.11:g.74285353G= , CM000666.1:g.74285353G=	GRCh37
NC_000004.10:g.74504217G=	NCBI36
NG_009291.1:g.20382G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1782G= MANE Select	ENSP00000295897.4:p.Glu594=
ENST00000295897.8:c.1782G=	ENSP00000295897.4:p.Glu594=
ENST00000401494.7:c.1437G=	ENSP00000384695.3:p.Glu479=
ENST00000415165.6:c.1206G=	ENSP00000401820.2:p.Glu402=
ENST00000476441.6:c.*1061G=	ENSP00000423727.1:n.*1061G=
ENST00000495173.1:n.90G=
ENST00000503124.5:c.1332G=	ENSP00000421027.1:p.Glu444=
ENST00000505649.5:n.1329G=
ENST00000508932.5:n.175+181G=
ENST00000509063.5:c.1782G=	ENSP00000422784.1:p.Glu594=
ENST00000511370.1:c.1315G=
ENST00000621085.4:c.1143G=	ENSP00000483421.1:p.Glu381=
ENST00000621628.4:c.1143G=	ENSP00000480485.1:p.Glu381=
NM_000477.5:c.1782G=	NP_000468.1:p.Glu594=
NM_000477.6:c.1782G=	NP_000468.1:p.Glu594=
NM_000477.7:c.1782G= MANE Select	NP_000468.1:p.Glu594=