Canonical Allele Identifier: CA645517871
Gene: ALB HGNC NCBI

Linked Data

COSMIC: COSM307306

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.73419571_73419574del , CM000666.2:g.73419571_73419574del GRCh38
NC_000004.11:g.74285288_74285291del , CM000666.1:g.74285288_74285291del GRCh37
NC_000004.10:g.74504152_74504155del NCBI36
NG_009291.1:g.20317_20320del

Transcript Alleles

HGVS Amino-acid Change
ENST00000295897.9:c.1717_1720del MANE Select ENSP00000295897.4:p.Asp573IlefsTer6
ENST00000295897.8:c.1717_1720del ENSP00000295897.4:p.Asp573IlefsTer6
ENST00000401494.7:c.1372_1375del ENSP00000384695.3:p.Asp458IlefsTer6
ENST00000415165.6:c.1141_1144del ENSP00000401820.2:p.Asp381IlefsTer6
ENST00000476441.6:c.*996_*999del ENSP00000423727.1:n.*996_*999del
ENST00000495173.1:n.25_28del
ENST00000503124.5:c.1267_1270del ENSP00000421027.1:p.Asp423IlefsTer6
ENST00000505649.5:n.1264_1267del
ENST00000508932.5:n.175+116_175+119del
ENST00000509063.5:c.1717_1720del ENSP00000422784.1:p.Asp573IlefsTer6
ENST00000511370.1:c.1250_1253del
ENST00000621085.4:c.1078_1081del ENSP00000483421.1:p.Asp360IlefsTer6
ENST00000621628.4:c.1078_1081del ENSP00000480485.1:p.Asp360IlefsTer6
NM_000477.5:c.1717_1720del NP_000468.1:p.Asp573IlefsTer6
NM_000477.6:c.1717_1720del NP_000468.1:p.Asp573IlefsTer6
NM_000477.7:c.1717_1720del MANE Select NP_000468.1:p.Asp573IlefsTer6