Canonical Allele Identifier: CA1468152392

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73408795T= , CM000666.2:g.73408795T=	GRCh38
NC_000004.11:g.74274512T= , CM000666.1:g.74274512T=	GRCh37
NC_000004.10:g.74493376T=	NCBI36
NG_009291.1:g.9541T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.472T= MANE Select	ENSP00000295897.4:p.Phe158=
ENST00000295897.8:c.472T=	ENSP00000295897.4:p.Phe158=
ENST00000401494.7:c.138-560T=	ENSP00000384695.3:n.138-560T=
ENST00000415165.6:c.138-3201T=	ENSP00000401820.2:n.138-3201T=
ENST00000441319.5:c.478T=	ENSP00000392541.1:p.Phe160=
ENST00000476441.6:c.80-560T=	ENSP00000423727.1:n.80-560T=
ENST00000503124.5:c.33-560T=	ENSP00000421027.1:n.33-560T=
ENST00000505649.5:n.158T=
ENST00000509063.5:c.472T=	ENSP00000422784.1:p.Phe158=
ENST00000510166.5:n.508T=
ENST00000514786.1:n.441T=
ENST00000515133.5:n.513T=
ENST00000621085.4:c.472T=	ENSP00000483421.1:p.Phe158=
ENST00000621628.4:c.472T=	ENSP00000480485.1:p.Phe158=
NM_000477.5:c.472T=	NP_000468.1:p.Phe158=
NM_000477.6:c.472T=	NP_000468.1:p.Phe158=
NM_000477.7:c.472T= MANE Select	NP_000468.1:p.Phe158=