Canonical Allele Identifier: CA1468150885

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406675G= , CM000666.2:g.73406675G=	GRCh38
NC_000004.11:g.74272392G= , CM000666.1:g.74272392G=	GRCh37
NC_000004.10:g.74491256G=	NCBI36
NG_009291.1:g.7421G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.184G= MANE Select	ENSP00000295897.4:p.Asp62=
ENST00000295897.8:c.184G=	ENSP00000295897.4:p.Asp62=
ENST00000401494.7:c.137+1502G=	ENSP00000384695.3:n.137+1502G=
ENST00000415165.6:c.137+1502G=	ENSP00000401820.2:n.137+1502G=
ENST00000441319.5:c.190G=	ENSP00000392541.1:p.Asp64=
ENST00000476441.6:c.79+2269G=	ENSP00000423727.1:n.79+2269G=
ENST00000503124.5:c.-55G=	ENSP00000421027.1:n.-55G=
ENST00000509063.5:c.184G=	ENSP00000422784.1:p.Asp62=
ENST00000510166.5:n.220G=
ENST00000514786.1:n.153G=
ENST00000515133.5:n.225G=
ENST00000621085.4:c.184G=	ENSP00000483421.1:p.Asp62=
ENST00000621628.4:c.184G=	ENSP00000480485.1:p.Asp62=
NM_000477.5:c.184G=	NP_000468.1:p.Asp62=
NM_000477.6:c.184G=	NP_000468.1:p.Asp62=
NM_000477.7:c.184G= MANE Select	NP_000468.1:p.Asp62=