Canonical Allele Identifier: CA1468148329

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419619G= , CM000666.2:g.73419619G=	GRCh38
NC_000004.11:g.74285336G= , CM000666.1:g.74285336G=	GRCh37
NC_000004.10:g.74504200G=	NCBI36
NG_009291.1:g.20365G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1765G= MANE Select	ENSP00000295897.4:p.Glu589=
ENST00000295897.8:c.1765G=	ENSP00000295897.4:p.Glu589=
ENST00000401494.7:c.1420G=	ENSP00000384695.3:p.Glu474=
ENST00000415165.6:c.1189G=	ENSP00000401820.2:p.Glu397=
ENST00000476441.6:c.*1044G=	ENSP00000423727.1:n.*1044G=
ENST00000495173.1:n.73G=
ENST00000503124.5:c.1315G=	ENSP00000421027.1:p.Glu439=
ENST00000505649.5:n.1312G=
ENST00000508932.5:n.175+164G=
ENST00000509063.5:c.1765G=	ENSP00000422784.1:p.Glu589=
ENST00000511370.1:c.1298G=
ENST00000621085.4:c.1126G=	ENSP00000483421.1:p.Glu376=
ENST00000621628.4:c.1126G=	ENSP00000480485.1:p.Glu376=
NM_000477.5:c.1765G=	NP_000468.1:p.Glu589=
NM_000477.6:c.1765G=	NP_000468.1:p.Glu589=
NM_000477.7:c.1765G= MANE Select	NP_000468.1:p.Glu589=