Canonical Allele Identifier: CA1504952247

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604906_154604907delinsTC , CM000666.2:g.154604906_154604907delinsTC	GRCh38
NC_000004.11:g.155526058_155526059delinsTC , CM000666.1:g.155526058_155526059delinsTC	GRCh37
NC_000004.10:g.155745508_155745509delinsTC	NCBI36
NG_008834.1:g.12844_12845delinsGA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1289_1290delinsGA MANE Select	ENSP00000336829.3:p.Gly430=
ENST00000336098.7:c.1289_1290delinsGA	ENSP00000336829.3:p.Gly430=
ENST00000404648.7:c.1289_1290delinsGA	ENSP00000384860.3:p.Gly430=
ENST00000405164.5:c.1313_1314delinsGA	ENSP00000384101.1:p.Gly438=
ENST00000407946.5:c.1313_1314delinsGA	ENSP00000384552.1:p.Gly438=
ENST00000465913.1:n.837_838delinsGA
ENST00000492082.5:n.1831_1832delinsGA
NM_000509.4:c.1289_1290delinsGA	NP_000500.2:p.Gly430=
NM_000509.5:c.1289_1290delinsGA	NP_000500.2:p.Gly430=
NM_021870.2:c.1289_1290delinsGA	NP_068656.2:p.Gly430=
NM_021870.3:c.1289_1290delinsGA MANE Select	NP_068656.2:p.Gly430=
NM_000509.6:c.1289_1290delinsGA	NP_000500.2:p.Gly430=