Canonical Allele Identifier: CA1468148828

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73420257A= , CM000666.2:g.73420257A=	GRCh38
NC_000004.11:g.74285974A= , CM000666.1:g.74285974A=	GRCh37
NC_000004.10:g.74504838A=	NCBI36
NG_009291.1:g.21003A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000295897.9:c.1789A= MANE Select	ENSP00000295897.4:p.Lys597=
ENST00000295897.8:c.1789A=	ENSP00000295897.4:p.Lys597=
ENST00000401494.7:c.1444A=	ENSP00000384695.3:p.Lys482=
ENST00000415165.6:c.1213A=	ENSP00000401820.2:p.Lys405=
ENST00000476441.6:c.*1068A=	ENSP00000423727.1:n.*1068A=
ENST00000495173.1:n.97A=
ENST00000503124.5:c.1339A=	ENSP00000421027.1:p.Lys447=
ENST00000505649.5:n.1336A=
ENST00000508932.5:n.179A=
ENST00000509063.5:c.1785+618A=	ENSP00000422784.1:n.1785+618A=
ENST00000511370.1:c.1322A=
ENST00000621085.4:c.1150A=	ENSP00000483421.1:p.Lys384=
ENST00000621628.4:c.1150A=	ENSP00000480485.1:p.Lys384=
NM_000477.5:c.1789A=	NP_000468.1:p.Lys597=
NM_000477.6:c.1789A=	NP_000468.1:p.Lys597=
NM_000477.7:c.1789A= MANE Select	NP_000468.1:p.Lys597=