Canonical Allele Identifier: CA1468144761

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73416280G= , CM000666.2:g.73416280G=	GRCh38
NC_000004.11:g.74281997G= , CM000666.1:g.74281997G=	GRCh37
NC_000004.10:g.74500861G=	NCBI36
NG_009291.1:g.17026G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1216G= MANE Select	NP_000468.1:p.Glu406=
ENST00000295897.9:c.1216G= MANE Select	ENSP00000295897.4:p.Glu406=
NM_000477.5:c.1216G=	NP_000468.1:p.Glu406=
NM_000477.6:c.1216G=	NP_000468.1:p.Glu406=
ENST00000295897.8:c.1216G=	ENSP00000295897.4:p.Glu406=
ENST00000401494.7:c.871G=	ENSP00000384695.3:p.Glu291=
ENST00000415165.6:c.640G=	ENSP00000401820.2:p.Glu214=
ENST00000476441.6:c.*495G=	ENSP00000423727.1:n.*495G=
ENST00000484992.1:n.536G=
ENST00000503124.5:c.766G=	ENSP00000421027.1:p.Glu256=
ENST00000505649.5:n.902G=
ENST00000509063.5:c.1216G=	ENSP00000422784.1:p.Glu406=
ENST00000511370.1:c.749G=
ENST00000621085.4:c.577G=	ENSP00000483421.1:p.Glu193=
ENST00000621628.4:c.577G=	ENSP00000480485.1:p.Glu193=