Canonical Allele Identifier: CA1468148214

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419567T= , CM000666.2:g.73419567T=	GRCh38
NC_000004.11:g.74285284T= , CM000666.1:g.74285284T=	GRCh37
NC_000004.10:g.74504148T=	NCBI36
NG_009291.1:g.20313T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1713T= MANE Select	ENSP00000295897.4:p.Val571=
ENST00000295897.8:c.1713T=	ENSP00000295897.4:p.Val571=
ENST00000401494.7:c.1368T=	ENSP00000384695.3:p.Val456=
ENST00000415165.6:c.1137T=	ENSP00000401820.2:p.Val379=
ENST00000476441.6:c.*992T=	ENSP00000423727.1:n.*992T=
ENST00000495173.1:n.21T=
ENST00000503124.5:c.1263T=	ENSP00000421027.1:p.Val421=
ENST00000505649.5:n.1260T=
ENST00000508932.5:n.175+112T=
ENST00000509063.5:c.1713T=	ENSP00000422784.1:p.Val571=
ENST00000511370.1:c.1246T=
ENST00000621085.4:c.1074T=	ENSP00000483421.1:p.Val358=
ENST00000621628.4:c.1074T=	ENSP00000480485.1:p.Val358=
NM_000477.5:c.1713T=	NP_000468.1:p.Val571=
NM_000477.6:c.1713T=	NP_000468.1:p.Val571=
NM_000477.7:c.1713T= MANE Select	NP_000468.1:p.Val571=