Canonical Allele Identifier: CA127922

Gene: ALB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.73419634G>A , CM000666.2:g.73419634G>A	GRCh38
NC_000004.11:g.74285351G>A , CM000666.1:g.74285351G>A	GRCh37
NC_000004.10:g.74504215G>A	NCBI36
NG_009291.1:g.20380G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_000477.7:c.1780G>A MANE Select	NP_000468.1:p.Glu594Lys
ENST00000295897.9:c.1780G>A MANE Select	ENSP00000295897.4:p.Glu594Lys
NM_000477.5:c.1780G>A	NP_000468.1:p.Glu594Lys
NM_000477.6:c.1780G>A	NP_000468.1:p.Glu594Lys
ENST00000295897.8:c.1780G>A	ENSP00000295897.4:p.Glu594Lys
ENST00000401494.7:c.1435G>A	ENSP00000384695.3:p.Glu479Lys
ENST00000415165.6:c.1204G>A	ENSP00000401820.2:p.Glu402Lys
ENST00000476441.6:c.*1059G>A	ENSP00000423727.1:n.*1059G>A
ENST00000495173.1:n.88G>A
ENST00000503124.5:c.1330G>A	ENSP00000421027.1:p.Glu444Lys
ENST00000505649.5:n.1327G>A
ENST00000508932.5:n.175+179G>A
ENST00000509063.5:c.1780G>A	ENSP00000422784.1:p.Glu594Lys
ENST00000511370.1:c.1313G>A
ENST00000621085.4:c.1141G>A	ENSP00000483421.1:p.Glu381Lys
ENST00000621628.4:c.1141G>A	ENSP00000480485.1:p.Glu381Lys