Canonical Allele Identifier: CA1468144727

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73416259G= , CM000666.2:g.73416259G=	GRCh38
NC_000004.11:g.74281976G= , CM000666.1:g.74281976G=	GRCh37
NC_000004.10:g.74500840G=	NCBI36
NG_009291.1:g.17005G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1195G= MANE Select	ENSP00000295897.4:p.Asp399=
ENST00000295897.8:c.1195G=	ENSP00000295897.4:p.Asp399=
ENST00000401494.7:c.850G=	ENSP00000384695.3:p.Asp284=
ENST00000415165.6:c.619G=	ENSP00000401820.2:p.Asp207=
ENST00000476441.6:c.*474G=	ENSP00000423727.1:n.*474G=
ENST00000484992.1:n.515G=
ENST00000503124.5:c.745G=	ENSP00000421027.1:p.Asp249=
ENST00000505649.5:n.881G=
ENST00000509063.5:c.1195G=	ENSP00000422784.1:p.Asp399=
ENST00000511370.1:c.728G=
ENST00000621085.4:c.556G=	ENSP00000483421.1:p.Asp186=
ENST00000621628.4:c.556G=	ENSP00000480485.1:p.Asp186=
NM_000477.5:c.1195G=	NP_000468.1:p.Asp399=
NM_000477.6:c.1195G=	NP_000468.1:p.Asp399=
NM_000477.7:c.1195G= MANE Select	NP_000468.1:p.Asp399=