Canonical Allele Identifier: CA1468148472

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404341C= , CM000666.2:g.73404341C=	GRCh38
NC_000004.11:g.74270058C= , CM000666.1:g.74270058C=	GRCh37
NC_000004.10:g.74488922C=	NCBI36
NG_009291.1:g.5087C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.14C= MANE Select	ENSP00000295897.4:p.Thr5=
ENST00000295897.8:c.14C=	ENSP00000295897.4:p.Thr5=
ENST00000401494.7:c.14C=	ENSP00000384695.3:p.Thr5=
ENST00000415165.6:c.14C=	ENSP00000401820.2:p.Thr5=
ENST00000441319.5:c.48-28C=	ENSP00000392541.1:n.48-28C=
ENST00000476441.6:c.14C=	ENSP00000423727.1:p.Thr5=
ENST00000503124.5:c.-167C=	ENSP00000421027.1:n.-167C=
ENST00000509063.5:c.14C=	ENSP00000422784.1:p.Thr5=
ENST00000510166.5:n.55C=
ENST00000514786.1:n.48+5C=
ENST00000515133.5:n.55C=
ENST00000621085.4:c.14C=	ENSP00000483421.1:p.Thr5=
ENST00000621628.4:c.14C=	ENSP00000480485.1:p.Thr5=
NM_000477.5:c.14C=	NP_000468.1:p.Thr5=
NM_000477.6:c.14C=	NP_000468.1:p.Thr5=
NM_000477.7:c.14C= MANE Select	NP_000468.1:p.Thr5=