Canonical Allele Identifier: CA1468152722

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409475C= , CM000666.2:g.73409475C=	GRCh38
NC_000004.11:g.74275192C= , CM000666.1:g.74275192C=	GRCh37
NC_000004.10:g.74494056C=	NCBI36
NG_009291.1:g.10221C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.603C= MANE Select	ENSP00000295897.4:p.Cys201=
ENST00000295897.8:c.603C=	ENSP00000295897.4:p.Cys201=
ENST00000401494.7:c.258C=	ENSP00000384695.3:p.Cys86=
ENST00000415165.6:c.138-2521C=	ENSP00000401820.2:n.138-2521C=
ENST00000476441.6:c.200C=	ENSP00000423727.1:p.Ala67=
ENST00000503124.5:c.153C=	ENSP00000421027.1:p.Cys51=
ENST00000505649.5:n.289C=
ENST00000509063.5:c.603C=	ENSP00000422784.1:p.Cys201=
ENST00000511370.1:c.136C=
ENST00000514786.1:n.572C=
ENST00000621085.4:c.490+113C=	ENSP00000483421.1:n.490+113C=
ENST00000621628.4:c.486+399C=	ENSP00000480485.1:n.486+399C=
NM_000477.5:c.603C=	NP_000468.1:p.Cys201=
NM_000477.6:c.603C=	NP_000468.1:p.Cys201=
NM_000477.7:c.603C= MANE Select	NP_000468.1:p.Cys201=