Canonical Allele Identifier: CA1468152721

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409474G= , CM000666.2:g.73409474G=	GRCh38
NC_000004.11:g.74275191G= , CM000666.1:g.74275191G=	GRCh37
NC_000004.10:g.74494055G=	NCBI36
NG_009291.1:g.10220G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.602G= MANE Select	ENSP00000295897.4:p.Cys201=
ENST00000295897.8:c.602G=	ENSP00000295897.4:p.Cys201=
ENST00000401494.7:c.257G=	ENSP00000384695.3:p.Cys86=
ENST00000415165.6:c.138-2522G=	ENSP00000401820.2:n.138-2522G=
ENST00000476441.6:c.199G=	ENSP00000423727.1:p.Ala67=
ENST00000503124.5:c.152G=	ENSP00000421027.1:p.Cys51=
ENST00000505649.5:n.288G=
ENST00000509063.5:c.602G=	ENSP00000422784.1:p.Cys201=
ENST00000511370.1:c.135G=
ENST00000514786.1:n.571G=
ENST00000621085.4:c.490+112G=	ENSP00000483421.1:n.490+112G=
ENST00000621628.4:c.486+398G=	ENSP00000480485.1:n.486+398G=
NM_000477.5:c.602G=	NP_000468.1:p.Cys201=
NM_000477.6:c.602G=	NP_000468.1:p.Cys201=
NM_000477.7:c.602G= MANE Select	NP_000468.1:p.Cys201=