Canonical Allele Identifier: CA2672444818
Gene: FGG HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.154604679_154604680insATATTTA , CM000666.2:g.154604679_154604680insATATTTA GRCh38
NC_000004.11:g.155525831_155525832insATATTTA , CM000666.1:g.155525831_155525832insATATTTA GRCh37
NC_000004.10:g.155745281_155745282insATATTTA NCBI36
NG_008834.1:g.13071_13072insTAAATAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000336098.8:c.*154_*155insTAAATAT MANE Select ENSP00000336829.3:n.*154_*155insTAAATAT
ENST00000336098.7:c.*154_*155insTAAATAT ENSP00000336829.3:n.*154_*155insTAAATAT
ENST00000404648.7:c.1299+217_1299+218insTAAATAT ENSP00000384860.3:n.1299+217_1299+218insTAAATAT
ENST00000405164.5:c.1323+217_1323+218insTAAATAT ENSP00000384101.1:n.1323+217_1323+218insTAAATAT
ENST00000407946.5:c.*154_*155insTAAATAT ENSP00000384552.1:n.*154_*155insTAAATAT
ENST00000465913.1:n.1064_1065insTAAATAT
ENST00000492082.5:n.1841+217_1841+218insTAAATAT
NM_000509.4:c.1299+217_1299+218insTAAATAT NP_000500.2:n.1299+217_1299+218insTAAATAT
NM_000509.5:c.1299+217_1299+218insTAAATAT NP_000500.2:n.1299+217_1299+218insTAAATAT
NM_021870.2:c.*154_*155insTAAATAT NP_068656.2:n.*154_*155insTAAATAT
NM_021870.3:c.*154_*155insTAAATAT MANE Select NP_068656.2:n.*154_*155insTAAATAT
NM_000509.6:c.1299+217_1299+218insTAAATAT NP_000500.2:n.1299+217_1299+218insTAAATAT