Canonical Allele Identifier: CA3115465
Gene: FGG HGNC NCBI

Linked Data

dbSNP Id: rs746473186

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604931_154604933del , CM000666.2:g.154604931_154604933del GRCh38
NC_000004.11:g.155526083_155526085del , CM000666.1:g.155526083_155526085del GRCh37
NC_000004.10:g.155745533_155745535del NCBI36
NG_008834.1:g.12820_12822del

Transcript Alleles

HGVS Amino-acid Change
ENST00000336098.8:c.1265_1267del MANE Select ENSP00000336829.3:p.Glu422del
ENST00000336098.7:c.1265_1267del ENSP00000336829.3:p.Glu422del
ENST00000404648.7:c.1265_1267del ENSP00000384860.3:p.Glu422del
ENST00000405164.5:c.1289_1291del ENSP00000384101.1:p.Glu430del
ENST00000407946.5:c.1289_1291del ENSP00000384552.1:p.Glu430del
ENST00000465913.1:n.813_815del
ENST00000492082.5:n.1807_1809del
NM_000509.4:c.1265_1267del NP_000500.2:p.Glu422del
NM_000509.5:c.1265_1267del NP_000500.2:p.Glu422del
NM_021870.2:c.1265_1267del NP_068656.2:p.Glu422del
NM_021870.3:c.1265_1267del MANE Select NP_068656.2:p.Glu422del
NM_000509.6:c.1265_1267del NP_000500.2:p.Glu422del