Canonical Allele Identifier: CA1504952176

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604716_154604724delinsAGGCTAAAT , CM000666.2:g.154604716_154604724delinsAGGCTAAAT	GRCh38
NC_000004.11:g.155525868_155525876delinsAGGCTAAAT , CM000666.1:g.155525868_155525876delinsAGGCTAAAT	GRCh37
NC_000004.10:g.155745318_155745326delinsAGGCTAAAT	NCBI36
NG_008834.1:g.13027_13035delinsATTTAGCCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.*110_*118delinsATTTAGCCT MANE Select	ENSP00000336829.3:n.*110_*118delinsATTTAGCCT
ENST00000336098.7:c.*110_*118delinsATTTAGCCT	ENSP00000336829.3:n.*110_*118delinsATTTAGCCT
ENST00000404648.7:c.1299+173_1299+181delinsATTTAGCCT	ENSP00000384860.3:n.1299+173_1299+181delinsATTTAGCCT
ENST00000405164.5:c.1323+173_1323+181delinsATTTAGCCT	ENSP00000384101.1:n.1323+173_1323+181delinsATTTAGCCT
ENST00000407946.5:c.*110_*118delinsATTTAGCCT	ENSP00000384552.1:n.*110_*118delinsATTTAGCCT
ENST00000465913.1:n.1020_1028delinsATTTAGCCT
ENST00000492082.5:n.1841+173_1841+181delinsATTTAGCCT
NM_000509.4:c.1299+173_1299+181delinsATTTAGCCT	NP_000500.2:n.1299+173_1299+181delinsATTTAGCCT
NM_000509.5:c.1299+173_1299+181delinsATTTAGCCT	NP_000500.2:n.1299+173_1299+181delinsATTTAGCCT
NM_021870.2:c.*110_*118delinsATTTAGCCT	NP_068656.2:n.*110_*118delinsATTTAGCCT
NM_021870.3:c.*110_*118delinsATTTAGCCT MANE Select	NP_068656.2:n.*110_*118delinsATTTAGCCT
NM_000509.6:c.1299+173_1299+181delinsATTTAGCCT	NP_000500.2:n.1299+173_1299+181delinsATTTAGCCT