Canonical Allele Identifier: CA1504952198

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604766_154604773delinsAAAAAAGG , CM000666.2:g.154604766_154604773delinsAAAAAAGG	GRCh38
NC_000004.11:g.155525918_155525925delinsAAAAAAGG , CM000666.1:g.155525918_155525925delinsAAAAAAGG	GRCh37
NC_000004.10:g.155745368_155745375delinsAAAAAAGG	NCBI36
NG_008834.1:g.12978_12985delinsCCTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.*61_*68delinsCCTTTTTT MANE Select	ENSP00000336829.3:n.*61_*68delinsCCTTTTTT
ENST00000336098.7:c.*61_*68delinsCCTTTTTT	ENSP00000336829.3:n.*61_*68delinsCCTTTTTT
ENST00000404648.7:c.1299+124_1299+131delinsCCTTTTTT	ENSP00000384860.3:n.1299+124_1299+131delinsCCTTTTTT
ENST00000405164.5:c.1323+124_1323+131delinsCCTTTTTT	ENSP00000384101.1:n.1323+124_1323+131delinsCCTTTTTT
ENST00000407946.5:c.*61_*68delinsCCTTTTTT	ENSP00000384552.1:n.*61_*68delinsCCTTTTTT
ENST00000465913.1:n.971_978delinsCCTTTTTT
ENST00000492082.5:n.1841+124_1841+131delinsCCTTTTTT
NM_000509.4:c.1299+124_1299+131delinsCCTTTTTT	NP_000500.2:n.1299+124_1299+131delinsCCTTTTTT
NM_000509.5:c.1299+124_1299+131delinsCCTTTTTT	NP_000500.2:n.1299+124_1299+131delinsCCTTTTTT
NM_021870.2:c.*61_*68delinsCCTTTTTT	NP_068656.2:n.*61_*68delinsCCTTTTTT
NM_021870.3:c.*61_*68delinsCCTTTTTT MANE Select	NP_068656.2:n.*61_*68delinsCCTTTTTT
NM_000509.6:c.1299+124_1299+131delinsCCTTTTTT	NP_000500.2:n.1299+124_1299+131delinsCCTTTTTT