Canonical Allele Identifier: CA1468141998

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413476G= , CM000666.2:g.73413476G=	GRCh38
NC_000004.11:g.74279193G= , CM000666.1:g.74279193G=	GRCh37
NC_000004.10:g.74498057G=	NCBI36
NG_009291.1:g.14222G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.900G= MANE Select	NP_000468.1:p.Lys300=
ENST00000295897.9:c.900G= MANE Select	ENSP00000295897.4:p.Lys300=
NM_000477.5:c.900G=	NP_000468.1:p.Lys300=
NM_000477.6:c.900G=	NP_000468.1:p.Lys300=
ENST00000295897.8:c.900G=	ENSP00000295897.4:p.Lys300=
ENST00000401494.7:c.555G=	ENSP00000384695.3:p.Lys185=
ENST00000415165.6:c.324G=	ENSP00000401820.2:p.Lys108=
ENST00000476441.6:c.*179G=	ENSP00000423727.1:n.*179G=
ENST00000484992.1:n.220G=
ENST00000503124.5:c.450G=	ENSP00000421027.1:p.Lys150=
ENST00000505649.5:n.586G=
ENST00000509063.5:c.900G=	ENSP00000422784.1:p.Lys300=
ENST00000511370.1:c.433G=
ENST00000621085.4:c.491-1630G=	ENSP00000483421.1:n.491-1630G=
ENST00000621628.4:c.487-1626G=	ENSP00000480485.1:n.487-1626G=