Canonical Allele Identifier: CA1468148281

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419601T= , CM000666.2:g.73419601T=	GRCh38
NC_000004.11:g.74285318T= , CM000666.1:g.74285318T=	GRCh37
NC_000004.10:g.74504182T=	NCBI36
NG_009291.1:g.20347T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1747T= MANE Select	ENSP00000295897.4:p.Cys583=
ENST00000295897.8:c.1747T=	ENSP00000295897.4:p.Cys583=
ENST00000401494.7:c.1402T=	ENSP00000384695.3:p.Cys468=
ENST00000415165.6:c.1171T=	ENSP00000401820.2:p.Cys391=
ENST00000476441.6:c.*1026T=	ENSP00000423727.1:n.*1026T=
ENST00000495173.1:n.55T=
ENST00000503124.5:c.1297T=	ENSP00000421027.1:p.Cys433=
ENST00000505649.5:n.1294T=
ENST00000508932.5:n.175+146T=
ENST00000509063.5:c.1747T=	ENSP00000422784.1:p.Cys583=
ENST00000511370.1:c.1280T=
ENST00000621085.4:c.1108T=	ENSP00000483421.1:p.Cys370=
ENST00000621628.4:c.1108T=	ENSP00000480485.1:p.Cys370=
NM_000477.5:c.1747T=	NP_000468.1:p.Cys583=
NM_000477.6:c.1747T=	NP_000468.1:p.Cys583=
NM_000477.7:c.1747T= MANE Select	NP_000468.1:p.Cys583=