Canonical Allele Identifier: CA108774379

Gene: FGG

Linked Data

• dbSNP Id: rs35443439

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604915del , CM000666.2:g.154604915del	GRCh38
NC_000004.11:g.155526067del , CM000666.1:g.155526067del	GRCh37
NC_000004.10:g.155745517del	NCBI36
NG_008834.1:g.12837del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1282del MANE Select	ENSP00000336829.3:p.Leu428TrpfsTer?
ENST00000336098.7:c.1282del	ENSP00000336829.3:p.Leu428TrpfsTer?
ENST00000404648.7:c.1282del	ENSP00000384860.3:p.Leu428TrpfsTer26
ENST00000405164.5:c.1306del	ENSP00000384101.1:p.Leu436TrpfsTer26
ENST00000407946.5:c.1306del	ENSP00000384552.1:p.Leu436TrpfsTer?
ENST00000465913.1:n.830del
ENST00000492082.5:n.1824del
NM_000509.4:c.1282del	NP_000500.2:p.Leu428TrpfsTer26
NM_000509.5:c.1282del	NP_000500.2:p.Leu428TrpfsTer26
NM_021870.2:c.1282del	NP_068656.2:p.Leu428TrpfsTer?
NM_021870.3:c.1282del MANE Select	NP_068656.2:p.Leu428TrpfsTer?
NM_000509.6:c.1282del	NP_000500.2:p.Leu428TrpfsTer26