Canonical Allele Identifier: CA2695203933

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604893del , CM000666.2:g.154604893del	GRCh38
NC_000004.11:g.155526045del , CM000666.1:g.155526045del	GRCh37
NC_000004.10:g.155745495del	NCBI36
NG_008834.1:g.12858del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1303del MANE Select	ENSP00000336829.3:p.Arg435AspfsTer28
ENST00000336098.7:c.1303del	ENSP00000336829.3:p.Arg435AspfsTer28
ENST00000404648.7:c.1299+4del	ENSP00000384860.3:n.1299+4del
ENST00000405164.5:c.1323+4del	ENSP00000384101.1:n.1323+4del
ENST00000407946.5:c.1327del	ENSP00000384552.1:p.Arg443AspfsTer28
ENST00000465913.1:n.851del
ENST00000492082.5:n.1841+4del
NM_000509.4:c.1299+4del	NP_000500.2:n.1299+4del
NM_000509.5:c.1299+4del	NP_000500.2:n.1299+4del
NM_021870.2:c.1303del	NP_068656.2:p.Arg435AspfsTer28
NM_021870.3:c.1303del MANE Select	NP_068656.2:p.Arg435AspfsTer28
NM_000509.6:c.1299+4del	NP_000500.2:n.1299+4del