Canonical Allele Identifier: CA1468143433

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415056A= , CM000666.2:g.73415056A=	GRCh38
NC_000004.11:g.74280773A= , CM000666.1:g.74280773A=	GRCh37
NC_000004.10:g.74499637A=	NCBI36
NG_009291.1:g.15802A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1080A= MANE Select	ENSP00000295897.4:p.Arg360=
ENST00000295897.8:c.1080A=	ENSP00000295897.4:p.Arg360=
ENST00000401494.7:c.735A=	ENSP00000384695.3:p.Arg245=
ENST00000415165.6:c.504A=	ENSP00000401820.2:p.Arg168=
ENST00000476441.6:c.*359A=	ENSP00000423727.1:n.*359A=
ENST00000484992.1:n.400A=
ENST00000503124.5:c.630A=	ENSP00000421027.1:p.Arg210=
ENST00000504043.1:n.83A=
ENST00000505649.5:n.766A=
ENST00000509063.5:c.1080A=	ENSP00000422784.1:p.Arg360=
ENST00000511370.1:c.613A=
ENST00000621085.4:c.491-50A=	ENSP00000483421.1:n.491-50A=
ENST00000621628.4:c.487-46A=	ENSP00000480485.1:n.487-46A=
NM_000477.5:c.1080A=	NP_000468.1:p.Arg360=
NM_000477.6:c.1080A=	NP_000468.1:p.Arg360=
NM_000477.7:c.1080A= MANE Select	NP_000468.1:p.Arg360=