Canonical Allele Identifier: CA2695203934

Gene: FGG

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604897del , CM000666.2:g.154604897del	GRCh38
NC_000004.11:g.155526049del , CM000666.1:g.155526049del	GRCh37
NC_000004.10:g.155745499del	NCBI36
NG_008834.1:g.12855del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1300del MANE Select	ENSP00000336829.3:p.Val434SerfsTer29
ENST00000336098.7:c.1300del	ENSP00000336829.3:p.Val434SerfsTer29
ENST00000404648.7:c.1299+1del
ENST00000405164.5:c.1323+1del
ENST00000407946.5:c.1324del	ENSP00000384552.1:p.Val442SerfsTer29
ENST00000465913.1:n.848del
ENST00000492082.5:n.1841+1del
NM_000509.4:c.1299+1del
NM_000509.5:c.1299+1del
NM_021870.2:c.1300del	NP_068656.2:p.Val434SerfsTer29
NM_021870.3:c.1300del MANE Select	NP_068656.2:p.Val434SerfsTer29
NM_000509.6:c.1299+1del