Canonical Allele Identifier: CA1468143596

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415135G= , CM000666.2:g.73415135G=	GRCh38
NC_000004.11:g.74280852G= , CM000666.1:g.74280852G=	GRCh37
NC_000004.10:g.74499716G=	NCBI36
NG_009291.1:g.15881G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000295897.9:c.1159G= MANE Select	ENSP00000295897.4:p.Ala387=
ENST00000295897.8:c.1159G=	ENSP00000295897.4:p.Ala387=
ENST00000401494.7:c.814G=	ENSP00000384695.3:p.Ala272=
ENST00000415165.6:c.583G=	ENSP00000401820.2:p.Ala195=
ENST00000476441.6:c.*438G=	ENSP00000423727.1:n.*438G=
ENST00000484992.1:n.479G=
ENST00000503124.5:c.709G=	ENSP00000421027.1:p.Ala237=
ENST00000504043.1:n.162G=
ENST00000505649.5:n.845G=
ENST00000509063.5:c.1159G=	ENSP00000422784.1:p.Ala387=
ENST00000511370.1:c.692G=
ENST00000621085.4:c.520G=	ENSP00000483421.1:p.Ala174=
ENST00000621628.4:c.520G=	ENSP00000480485.1:p.Ala174=
NM_000477.5:c.1159G=	NP_000468.1:p.Ala387=
NM_000477.6:c.1159G=	NP_000468.1:p.Ala387=
NM_000477.7:c.1159G= MANE Select	NP_000468.1:p.Ala387=