Canonical Allele Identifier: CA1468148302

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419612C= , CM000666.2:g.73419612C=	GRCh38
NC_000004.11:g.74285329C= , CM000666.1:g.74285329C=	GRCh37
NC_000004.10:g.74504193C=	NCBI36
NG_009291.1:g.20358C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1758C= MANE Select	ENSP00000295897.4:p.Asp586=
ENST00000295897.8:c.1758C=	ENSP00000295897.4:p.Asp586=
ENST00000401494.7:c.1413C=	ENSP00000384695.3:p.Asp471=
ENST00000415165.6:c.1182C=	ENSP00000401820.2:p.Asp394=
ENST00000476441.6:c.*1037C=	ENSP00000423727.1:n.*1037C=
ENST00000495173.1:n.66C=
ENST00000503124.5:c.1308C=	ENSP00000421027.1:p.Asp436=
ENST00000505649.5:n.1305C=
ENST00000508932.5:n.175+157C=
ENST00000509063.5:c.1758C=	ENSP00000422784.1:p.Asp586=
ENST00000511370.1:c.1291C=
ENST00000621085.4:c.1119C=	ENSP00000483421.1:p.Asp373=
ENST00000621628.4:c.1119C=	ENSP00000480485.1:p.Asp373=
NM_000477.5:c.1758C=	NP_000468.1:p.Asp586=
NM_000477.6:c.1758C=	NP_000468.1:p.Asp586=
NM_000477.7:c.1758C= MANE Select	NP_000468.1:p.Asp586=