Canonical Allele Identifier: CA1468141966

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73413455T= , CM000666.2:g.73413455T=	GRCh38
NC_000004.11:g.74279172T= , CM000666.1:g.74279172T=	GRCh37
NC_000004.10:g.74498036T=	NCBI36
NG_009291.1:g.14201T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.879T= MANE Select	ENSP00000295897.4:p.Asp293=
ENST00000295897.8:c.879T=	ENSP00000295897.4:p.Asp293=
ENST00000401494.7:c.534T=	ENSP00000384695.3:p.Asp178=
ENST00000415165.6:c.303T=	ENSP00000401820.2:p.Asp101=
ENST00000476441.6:c.*158T=	ENSP00000423727.1:n.*158T=
ENST00000484992.1:n.199T=
ENST00000503124.5:c.429T=	ENSP00000421027.1:p.Asp143=
ENST00000505649.5:n.565T=
ENST00000509063.5:c.879T=	ENSP00000422784.1:p.Asp293=
ENST00000511370.1:c.412T=
ENST00000621085.4:c.491-1651T=	ENSP00000483421.1:n.491-1651T=
ENST00000621628.4:c.487-1647T=	ENSP00000480485.1:n.487-1647T=
NM_000477.5:c.879T=	NP_000468.1:p.Asp293=
NM_000477.6:c.879T=	NP_000468.1:p.Asp293=
NM_000477.7:c.879T= MANE Select	NP_000468.1:p.Asp293=