Canonical Allele Identifier: CA1468150990

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73406758A= , CM000666.2:g.73406758A=	GRCh38
NC_000004.11:g.74272475A= , CM000666.1:g.74272475A=	GRCh37
NC_000004.10:g.74491339A=	NCBI36
NG_009291.1:g.7504A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.267A= MANE Select	ENSP00000295897.4:p.Ser89=
ENST00000295897.8:c.267A=	ENSP00000295897.4:p.Ser89=
ENST00000401494.7:c.137+1585A=	ENSP00000384695.3:n.137+1585A=
ENST00000415165.6:c.137+1585A=	ENSP00000401820.2:n.137+1585A=
ENST00000441319.5:c.273A=	ENSP00000392541.1:p.Ser91=
ENST00000476441.6:c.79+2352A=	ENSP00000423727.1:n.79+2352A=
ENST00000503124.5:c.29A=	ENSP00000421027.1:p.His10=
ENST00000509063.5:c.267A=	ENSP00000422784.1:p.Ser89=
ENST00000510166.5:n.303A=
ENST00000514786.1:n.236A=
ENST00000515133.5:n.308A=
ENST00000621085.4:c.267A=	ENSP00000483421.1:p.Ser89=
ENST00000621628.4:c.267A=	ENSP00000480485.1:p.Ser89=
NM_000477.5:c.267A=	NP_000468.1:p.Ser89=
NM_000477.6:c.267A=	NP_000468.1:p.Ser89=
NM_000477.7:c.267A= MANE Select	NP_000468.1:p.Ser89=