Canonical Allele Identifier: CA1468152379

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408769C= , CM000666.2:g.73408769C=	GRCh38
NC_000004.11:g.74274486C= , CM000666.1:g.74274486C=	GRCh37
NC_000004.10:g.74493350C=	NCBI36
NG_009291.1:g.9515C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.446C= MANE Select	ENSP00000295897.4:p.Thr149=
ENST00000295897.8:c.446C=	ENSP00000295897.4:p.Thr149=
ENST00000401494.7:c.138-586C=	ENSP00000384695.3:n.138-586C=
ENST00000415165.6:c.138-3227C=	ENSP00000401820.2:n.138-3227C=
ENST00000441319.5:c.452C=	ENSP00000392541.1:p.Thr151=
ENST00000476441.6:c.80-586C=	ENSP00000423727.1:n.80-586C=
ENST00000503124.5:c.33-586C=	ENSP00000421027.1:n.33-586C=
ENST00000505649.5:n.132C=
ENST00000509063.5:c.446C=	ENSP00000422784.1:p.Thr149=
ENST00000510166.5:n.482C=
ENST00000514786.1:n.415C=
ENST00000515133.5:n.487C=
ENST00000621085.4:c.446C=	ENSP00000483421.1:p.Thr149=
ENST00000621628.4:c.446C=	ENSP00000480485.1:p.Thr149=
NM_000477.5:c.446C=	NP_000468.1:p.Thr149=
NM_000477.6:c.446C=	NP_000468.1:p.Thr149=
NM_000477.7:c.446C= MANE Select	NP_000468.1:p.Thr149=