Canonical Allele Identifier: CA2707339012
Gene: FGG HGNC NCBI

Linked Data

dbSNP Id: rs2110838371
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604754del , CM000666.2:g.154604754del GRCh38
NC_000004.11:g.155525906del , CM000666.1:g.155525906del GRCh37
NC_000004.10:g.155745356del NCBI36
NG_008834.1:g.12999del

Transcript Alleles

HGVS Amino-acid change
ENST00000336098.8:c.*82del MANE Select ENSP00000336829.3:n.*82del
ENST00000336098.7:c.*82del ENSP00000336829.3:n.*82del
ENST00000404648.7:c.1299+145del ENSP00000384860.3:n.1299+145del
ENST00000405164.5:c.1323+145del ENSP00000384101.1:n.1323+145del
ENST00000407946.5:c.*82del ENSP00000384552.1:n.*82del
ENST00000465913.1:n.992del
ENST00000492082.5:n.1841+145del
NM_000509.4:c.1299+145del NP_000500.2:n.1299+145del
NM_000509.5:c.1299+145del NP_000500.2:n.1299+145del
NM_021870.2:c.*82del NP_068656.2:n.*82del
NM_021870.3:c.*82del MANE Select NP_068656.2:n.*82del
NM_000509.6:c.1299+145del NP_000500.2:n.1299+145del
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