Canonical Allele Identifier: CA789378566

Gene: FGG

Linked Data

• dbSNP Id: rs1251150021
• MyVariant Identifiers: chr4:g.155525919_155525925del (hg19) ; chr4:g.154604767_154604773del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604769_154604775del , CM000666.2:g.154604769_154604775del	GRCh38
NC_000004.11:g.155525921_155525927del , CM000666.1:g.155525921_155525927del	GRCh37
NC_000004.10:g.155745371_155745377del	NCBI36
NG_008834.1:g.12978_12984del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.*61_*67del MANE Select	ENSP00000336829.3:n.*61_*67del
ENST00000336098.7:c.*61_*67del	ENSP00000336829.3:n.*61_*67del
ENST00000404648.7:c.1299+124_1299+130del	ENSP00000384860.3:n.1299+124_1299+130del
ENST00000405164.5:c.1323+124_1323+130del	ENSP00000384101.1:n.1323+124_1323+130del
ENST00000407946.5:c.*61_*67del	ENSP00000384552.1:n.*61_*67del
ENST00000465913.1:n.971_977del
ENST00000492082.5:n.1841+124_1841+130del
NM_000509.4:c.1299+124_1299+130del	NP_000500.2:n.1299+124_1299+130del
NM_000509.5:c.1299+124_1299+130del	NP_000500.2:n.1299+124_1299+130del
NM_021870.2:c.*61_*67del	NP_068656.2:n.*61_*67del
NM_021870.3:c.*61_*67del MANE Select	NP_068656.2:n.*61_*67del
NM_000509.6:c.1299+124_1299+130del	NP_000500.2:n.1299+124_1299+130del