Canonical Allele Identifier: CA1468152703

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73409432C= , CM000666.2:g.73409432C=	GRCh38
NC_000004.11:g.74275149C= , CM000666.1:g.74275149C=	GRCh37
NC_000004.10:g.74494013C=	NCBI36
NG_009291.1:g.10178C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.560C= MANE Select	ENSP00000295897.4:p.Ala187=
ENST00000295897.8:c.560C=	ENSP00000295897.4:p.Ala187=
ENST00000401494.7:c.215C=	ENSP00000384695.3:p.Ala72=
ENST00000415165.6:c.138-2564C=	ENSP00000401820.2:n.138-2564C=
ENST00000441319.5:c.566C=	ENSP00000392541.1:p.Ala189=
ENST00000476441.6:c.157C=	ENSP00000423727.1:p.Leu53=
ENST00000503124.5:c.110C=	ENSP00000421027.1:p.Ala37=
ENST00000505649.5:n.246C=
ENST00000509063.5:c.560C=	ENSP00000422784.1:p.Ala187=
ENST00000511370.1:c.93C=
ENST00000514786.1:n.529C=
ENST00000621085.4:c.490+70C=	ENSP00000483421.1:n.490+70C=
ENST00000621628.4:c.486+356C=	ENSP00000480485.1:n.486+356C=
NM_000477.5:c.560C=	NP_000468.1:p.Ala187=
NM_000477.6:c.560C=	NP_000468.1:p.Ala187=
NM_000477.7:c.560C= MANE Select	NP_000468.1:p.Ala187=