Canonical Allele Identifier: CA1468148099

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419514G= , CM000666.2:g.73419514G=	GRCh38
NC_000004.11:g.74285231G= , CM000666.1:g.74285231G=	GRCh37
NC_000004.10:g.74504095G=	NCBI36
NG_009291.1:g.20260G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1660G= MANE Select	ENSP00000295897.4:p.Val554=
ENST00000295897.8:c.1660G=	ENSP00000295897.4:p.Val554=
ENST00000401494.7:c.1315G=	ENSP00000384695.3:p.Val439=
ENST00000415165.6:c.1084G=	ENSP00000401820.2:p.Val362=
ENST00000476441.6:c.*939G=	ENSP00000423727.1:n.*939G=
ENST00000486939.1:n.314G=
ENST00000503124.5:c.1210G=	ENSP00000421027.1:p.Val404=
ENST00000505649.5:n.1207G=
ENST00000508932.5:n.175+59G=
ENST00000509063.5:c.1660G=	ENSP00000422784.1:p.Val554=
ENST00000511370.1:c.1193G=
ENST00000621085.4:c.1021G=	ENSP00000483421.1:p.Val341=
ENST00000621628.4:c.1021G=	ENSP00000480485.1:p.Val341=
NM_000477.5:c.1660G=	NP_000468.1:p.Val554=
NM_000477.6:c.1660G=	NP_000468.1:p.Val554=
NM_000477.7:c.1660G= MANE Select	NP_000468.1:p.Val554=