Canonical Allele Identifier: CA1468146833

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418143A= , CM000666.2:g.73418143A=	GRCh38
NC_000004.11:g.74283860A= , CM000666.1:g.74283860A=	GRCh37
NC_000004.10:g.74502724A=	NCBI36
NG_009291.1:g.18889A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1484A= MANE Select	ENSP00000295897.4:p.Asp495=
ENST00000295897.8:c.1484A=	ENSP00000295897.4:p.Asp495=
ENST00000401494.7:c.1139A=	ENSP00000384695.3:p.Asp380=
ENST00000415165.6:c.908A=	ENSP00000401820.2:p.Asp303=
ENST00000476441.6:c.*763A=	ENSP00000423727.1:n.*763A=
ENST00000486939.1:n.138A=
ENST00000503124.5:c.1034A=	ENSP00000421027.1:p.Asp345=
ENST00000505649.5:n.1031A=
ENST00000509063.5:c.1484A=	ENSP00000422784.1:p.Asp495=
ENST00000511370.1:c.1017A=
ENST00000621085.4:c.845A=	ENSP00000483421.1:p.Asp282=
ENST00000621628.4:c.845A=	ENSP00000480485.1:p.Asp282=
NM_000477.5:c.1484A=	NP_000468.1:p.Asp495=
NM_000477.6:c.1484A=	NP_000468.1:p.Asp495=
NM_000477.7:c.1484A= MANE Select	NP_000468.1:p.Asp495=