Canonical Allele Identifier: CA1468152672

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409376A= , CM000666.2:g.73409376A=	GRCh38
NC_000004.11:g.74275093A= , CM000666.1:g.74275093A=	GRCh37
NC_000004.10:g.74493957A=	NCBI36
NG_009291.1:g.10122A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.504A= MANE Select	ENSP00000295897.4:p.Arg168=
ENST00000295897.8:c.504A=	ENSP00000295897.4:p.Arg168=
ENST00000401494.7:c.159A=	ENSP00000384695.3:p.Arg53=
ENST00000415165.6:c.138-2620A=	ENSP00000401820.2:n.138-2620A=
ENST00000441319.5:c.510A=	ENSP00000392541.1:p.Arg170=
ENST00000476441.6:c.101A=	ENSP00000423727.1:p.Glu34=
ENST00000503124.5:c.54A=	ENSP00000421027.1:p.Arg18=
ENST00000505649.5:n.190A=
ENST00000509063.5:c.504A=	ENSP00000422784.1:p.Arg168=
ENST00000511370.1:c.37A=
ENST00000514786.1:n.473A=
ENST00000621085.4:c.490+14A=	ENSP00000483421.1:n.490+14A=
ENST00000621628.4:c.486+300A=	ENSP00000480485.1:n.486+300A=
NM_000477.5:c.504A=	NP_000468.1:p.Arg168=
NM_000477.6:c.504A=	NP_000468.1:p.Arg168=
NM_000477.7:c.504A= MANE Select	NP_000468.1:p.Arg168=