Canonical Allele Identifier: CA1468146948

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418262G= , CM000666.2:g.73418262G=	GRCh38
NC_000004.11:g.74283979G= , CM000666.1:g.74283979G=	GRCh37
NC_000004.10:g.74502843G=	NCBI36
NG_009291.1:g.19008G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1603G= MANE Select	ENSP00000295897.4:p.Ala535=
ENST00000295897.8:c.1603G=	ENSP00000295897.4:p.Ala535=
ENST00000401494.7:c.1258G=	ENSP00000384695.3:p.Ala420=
ENST00000415165.6:c.1027G=	ENSP00000401820.2:p.Ala343=
ENST00000476441.6:c.*882G=	ENSP00000423727.1:n.*882G=
ENST00000486939.1:n.257G=
ENST00000503124.5:c.1153G=	ENSP00000421027.1:p.Ala385=
ENST00000505649.5:n.1150G=
ENST00000509063.5:c.1603G=	ENSP00000422784.1:p.Ala535=
ENST00000511370.1:c.1136G=
ENST00000621085.4:c.964G=	ENSP00000483421.1:p.Ala322=
ENST00000621628.4:c.964G=	ENSP00000480485.1:p.Ala322=
NM_000477.5:c.1603G=	NP_000468.1:p.Ala535=
NM_000477.6:c.1603G=	NP_000468.1:p.Ala535=
NM_000477.7:c.1603G= MANE Select	NP_000468.1:p.Ala535=