Canonical Allele Identifier: CA1468152716

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409462A= , CM000666.2:g.73409462A=	GRCh38
NC_000004.11:g.74275179A= , CM000666.1:g.74275179A=	GRCh37
NC_000004.10:g.74494043A=	NCBI36
NG_009291.1:g.10208A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.590A= MANE Select	ENSP00000295897.4:p.Asp197=
ENST00000295897.8:c.590A=	ENSP00000295897.4:p.Asp197=
ENST00000401494.7:c.245A=	ENSP00000384695.3:p.Asp82=
ENST00000415165.6:c.138-2534A=	ENSP00000401820.2:n.138-2534A=
ENST00000476441.6:c.187A=	ENSP00000423727.1:p.Ile63=
ENST00000503124.5:c.140A=	ENSP00000421027.1:p.Asp47=
ENST00000505649.5:n.276A=
ENST00000509063.5:c.590A=	ENSP00000422784.1:p.Asp197=
ENST00000511370.1:c.123A=
ENST00000514786.1:n.559A=
ENST00000621085.4:c.490+100A=	ENSP00000483421.1:n.490+100A=
ENST00000621628.4:c.486+386A=	ENSP00000480485.1:n.486+386A=
NM_000477.5:c.590A=	NP_000468.1:p.Asp197=
NM_000477.6:c.590A=	NP_000468.1:p.Asp197=
NM_000477.7:c.590A= MANE Select	NP_000468.1:p.Asp197=