Canonical Allele Identifier: CA2580071797
Gene: ALB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73418231del , CM000666.2:g.73418231del GRCh38
NC_000004.11:g.74283948del , CM000666.1:g.74283948del GRCh37
NC_000004.10:g.74502812del NCBI36
NG_009291.1:g.18977del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1572del MANE Select ENSP00000295897.4:p.Glu525SerfsTer?
ENST00000295897.8:c.1572del ENSP00000295897.4:p.Glu525SerfsTer?
ENST00000401494.7:c.1227del ENSP00000384695.3:p.Glu410SerfsTer?
ENST00000415165.6:c.996del ENSP00000401820.2:p.Glu333SerfsTer?
ENST00000476441.6:c.*851del ENSP00000423727.1:n.*851del
ENST00000486939.1:n.226del
ENST00000503124.5:c.1122del ENSP00000421027.1:p.Glu375SerfsTer?
ENST00000505649.5:n.1119del
ENST00000509063.5:c.1572del ENSP00000422784.1:p.Glu525SerfsTer?
ENST00000511370.1:c.1105del
ENST00000621085.4:c.933del ENSP00000483421.1:p.Glu312SerfsTer?
ENST00000621628.4:c.933del ENSP00000480485.1:p.Glu312SerfsTer?
NM_000477.5:c.1572del NP_000468.1:p.Glu525SerfsTer?
NM_000477.6:c.1572del NP_000468.1:p.Glu525SerfsTer?
NM_000477.7:c.1572del MANE Select NP_000468.1:p.Glu525SerfsTer?