Canonical Allele Identifier: CA1468141983

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413466G= , CM000666.2:g.73413466G=	GRCh38
NC_000004.11:g.74279183G= , CM000666.1:g.74279183G=	GRCh37
NC_000004.10:g.74498047G=	NCBI36
NG_009291.1:g.14212G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.890G= MANE Select	ENSP00000295897.4:p.Ser297=
ENST00000295897.8:c.890G=	ENSP00000295897.4:p.Ser297=
ENST00000401494.7:c.545G=	ENSP00000384695.3:p.Ser182=
ENST00000415165.6:c.314G=	ENSP00000401820.2:p.Ser105=
ENST00000476441.6:c.*169G=	ENSP00000423727.1:n.*169G=
ENST00000484992.1:n.210G=
ENST00000503124.5:c.440G=	ENSP00000421027.1:p.Ser147=
ENST00000505649.5:n.576G=
ENST00000509063.5:c.890G=	ENSP00000422784.1:p.Ser297=
ENST00000511370.1:c.423G=
ENST00000621085.4:c.491-1640G=	ENSP00000483421.1:n.491-1640G=
ENST00000621628.4:c.487-1636G=	ENSP00000480485.1:n.487-1636G=
NM_000477.5:c.890G=	NP_000468.1:p.Ser297=
NM_000477.6:c.890G=	NP_000468.1:p.Ser297=
NM_000477.7:c.890G= MANE Select	NP_000468.1:p.Ser297=