Canonical Allele Identifier: CA1468150952

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406729G= , CM000666.2:g.73406729G=	GRCh38
NC_000004.11:g.74272446G= , CM000666.1:g.74272446G=	GRCh37
NC_000004.10:g.74491310G=	NCBI36
NG_009291.1:g.7475G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.238G= MANE Select	ENSP00000295897.4:p.Asp80=
ENST00000295897.8:c.238G=	ENSP00000295897.4:p.Asp80=
ENST00000401494.7:c.137+1556G=	ENSP00000384695.3:n.137+1556G=
ENST00000415165.6:c.137+1556G=	ENSP00000401820.2:n.137+1556G=
ENST00000441319.5:c.244G=	ENSP00000392541.1:p.Asp82=
ENST00000476441.6:c.79+2323G=	ENSP00000423727.1:n.79+2323G=
ENST00000503124.5:c.-1G=	ENSP00000421027.1:n.-1G=
ENST00000509063.5:c.238G=	ENSP00000422784.1:p.Asp80=
ENST00000510166.5:n.274G=
ENST00000514786.1:n.207G=
ENST00000515133.5:n.279G=
ENST00000621085.4:c.238G=	ENSP00000483421.1:p.Asp80=
ENST00000621628.4:c.238G=	ENSP00000480485.1:p.Asp80=
NM_000477.5:c.238G=	NP_000468.1:p.Asp80=
NM_000477.6:c.238G=	NP_000468.1:p.Asp80=
NM_000477.7:c.238G= MANE Select	NP_000468.1:p.Asp80=