Canonical Allele Identifier: CA1468142218

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413609G= , CM000666.2:g.73413609G=	GRCh38
NC_000004.11:g.74279326G= , CM000666.1:g.74279326G=	GRCh37
NC_000004.10:g.74498190G=	NCBI36
NG_009291.1:g.14355G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1033G= MANE Select	NP_000468.1:p.Glu345=
ENST00000295897.9:c.1033G= MANE Select	ENSP00000295897.4:p.Glu345=
NM_000477.5:c.1033G=	NP_000468.1:p.Glu345=
NM_000477.6:c.1033G=	NP_000468.1:p.Glu345=
ENST00000295897.8:c.1033G=	ENSP00000295897.4:p.Glu345=
ENST00000401494.7:c.688G=	ENSP00000384695.3:p.Glu230=
ENST00000415165.6:c.457G=	ENSP00000401820.2:p.Glu153=
ENST00000476441.6:c.*312G=	ENSP00000423727.1:n.*312G=
ENST00000484992.1:n.353G=
ENST00000503124.5:c.583G=	ENSP00000421027.1:p.Glu195=
ENST00000504043.1:n.36G=
ENST00000505649.5:n.719G=
ENST00000509063.5:c.1033G=	ENSP00000422784.1:p.Glu345=
ENST00000511370.1:c.566G=
ENST00000621085.4:c.491-1497G=	ENSP00000483421.1:n.491-1497G=
ENST00000621628.4:c.487-1493G=	ENSP00000480485.1:n.487-1493G=