Canonical Allele Identifier: CA1468146914

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73418218C= , CM000666.2:g.73418218C=	GRCh38
NC_000004.11:g.74283935C= , CM000666.1:g.74283935C=	GRCh37
NC_000004.10:g.74502799C=	NCBI36
NG_009291.1:g.18964C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1559C= MANE Select	ENSP00000295897.4:p.Thr520=
ENST00000295897.8:c.1559C=	ENSP00000295897.4:p.Thr520=
ENST00000401494.7:c.1214C=	ENSP00000384695.3:p.Thr405=
ENST00000415165.6:c.983C=	ENSP00000401820.2:p.Thr328=
ENST00000476441.6:c.*838C=	ENSP00000423727.1:n.*838C=
ENST00000486939.1:n.213C=
ENST00000503124.5:c.1109C=	ENSP00000421027.1:p.Thr370=
ENST00000505649.5:n.1106C=
ENST00000509063.5:c.1559C=	ENSP00000422784.1:p.Thr520=
ENST00000511370.1:c.1092C=
ENST00000621085.4:c.920C=	ENSP00000483421.1:p.Thr307=
ENST00000621628.4:c.920C=	ENSP00000480485.1:p.Thr307=
NM_000477.5:c.1559C=	NP_000468.1:p.Thr520=
NM_000477.6:c.1559C=	NP_000468.1:p.Thr520=
NM_000477.7:c.1559C= MANE Select	NP_000468.1:p.Thr520=