Canonical Allele Identifier: CA1468143436

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73415059G= , CM000666.2:g.73415059G=	GRCh38
NC_000004.11:g.74280776G= , CM000666.1:g.74280776G=	GRCh37
NC_000004.10:g.74499640G=	NCBI36
NG_009291.1:g.15805G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1083G= MANE Select	ENSP00000295897.4:p.Arg361=
ENST00000295897.8:c.1083G=	ENSP00000295897.4:p.Arg361=
ENST00000401494.7:c.738G=	ENSP00000384695.3:p.Arg246=
ENST00000415165.6:c.507G=	ENSP00000401820.2:p.Arg169=
ENST00000476441.6:c.*362G=	ENSP00000423727.1:n.*362G=
ENST00000484992.1:n.403G=
ENST00000503124.5:c.633G=	ENSP00000421027.1:p.Arg211=
ENST00000504043.1:n.86G=
ENST00000505649.5:n.769G=
ENST00000509063.5:c.1083G=	ENSP00000422784.1:p.Arg361=
ENST00000511370.1:c.616G=
ENST00000621085.4:c.491-47G=	ENSP00000483421.1:n.491-47G=
ENST00000621628.4:c.487-43G=	ENSP00000480485.1:n.487-43G=
NM_000477.5:c.1083G=	NP_000468.1:p.Arg361=
NM_000477.6:c.1083G=	NP_000468.1:p.Arg361=
NM_000477.7:c.1083G= MANE Select	NP_000468.1:p.Arg361=