Canonical Allele Identifier: CA1504952148

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604647_154604648delinsCA , CM000666.2:g.154604647_154604648delinsCA	GRCh38
NC_000004.11:g.155525799_155525800delinsCA , CM000666.1:g.155525799_155525800delinsCA	GRCh37
NC_000004.10:g.155745249_155745250delinsCA	NCBI36
NG_008834.1:g.13103_13104delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.*186_*187delinsTG MANE Select	ENSP00000336829.3:n.*186_*187delinsTG
ENST00000336098.7:c.*186_*187delinsTG	ENSP00000336829.3:n.*186_*187delinsTG
ENST00000404648.7:c.1299+249_1299+250delinsTG	ENSP00000384860.3:n.1299+249_1299+250delinsTG
ENST00000405164.5:c.1323+249_1323+250delinsTG	ENSP00000384101.1:n.1323+249_1323+250delinsTG
ENST00000407946.5:c.*186_*187delinsTG	ENSP00000384552.1:n.*186_*187delinsTG
ENST00000465913.1:n.1096_1097delinsTG
ENST00000492082.5:n.1841+249_1841+250delinsTG
NM_000509.4:c.1299+249_1299+250delinsTG	NP_000500.2:n.1299+249_1299+250delinsTG
NM_000509.5:c.1299+249_1299+250delinsTG	NP_000500.2:n.1299+249_1299+250delinsTG
NM_021870.2:c.*186_*187delinsTG	NP_068656.2:n.*186_*187delinsTG
NM_021870.3:c.*186_*187delinsTG MANE Select	NP_068656.2:n.*186_*187delinsTG
NM_000509.6:c.1299+249_1299+250delinsTG	NP_000500.2:n.1299+249_1299+250delinsTG