Canonical Allele Identifier: CA1468148503

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73404359T= , CM000666.2:g.73404359T=	GRCh38
NC_000004.11:g.74270076T= , CM000666.1:g.74270076T=	GRCh37
NC_000004.10:g.74488940T=	NCBI36
NG_009291.1:g.5105T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.32T= MANE Select	ENSP00000295897.4:p.Phe11=
ENST00000295897.8:c.32T=	ENSP00000295897.4:p.Phe11=
ENST00000401494.7:c.32T=	ENSP00000384695.3:p.Phe11=
ENST00000415165.6:c.32T=	ENSP00000401820.2:p.Phe11=
ENST00000441319.5:c.48-10T=	ENSP00000392541.1:n.48-10T=
ENST00000476441.6:c.32T=	ENSP00000423727.1:p.Phe11=
ENST00000503124.5:c.-149T=	ENSP00000421027.1:n.-149T=
ENST00000509063.5:c.32T=	ENSP00000422784.1:p.Phe11=
ENST00000510166.5:n.73T=
ENST00000514786.1:n.48+23T=
ENST00000515133.5:n.73T=
ENST00000621085.4:c.32T=	ENSP00000483421.1:p.Phe11=
ENST00000621628.4:c.32T=	ENSP00000480485.1:p.Phe11=
NM_000477.5:c.32T=	NP_000468.1:p.Phe11=
NM_000477.6:c.32T=	NP_000468.1:p.Phe11=
NM_000477.7:c.32T= MANE Select	NP_000468.1:p.Phe11=