Canonical Allele Identifier: CA789378536

Gene: FGG

Linked Data

• dbSNP Id: rs1177593345
• MyVariant Identifiers: chr4:g.155525869_155525876del (hg19) ; chr4:g.154604717_154604724del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604718_154604725del , CM000666.2:g.154604718_154604725del	GRCh38
NC_000004.11:g.155525870_155525877del , CM000666.1:g.155525870_155525877del	GRCh37
NC_000004.10:g.155745320_155745327del	NCBI36
NG_008834.1:g.13027_13034del

Transcript Alleles

HGVS	Amino-acid change
ENST00000336098.8:c.*110_*117del MANE Select	ENSP00000336829.3:n.*110_*117del
ENST00000336098.7:c.*110_*117del	ENSP00000336829.3:n.*110_*117del
ENST00000404648.7:c.1299+173_1299+180del	ENSP00000384860.3:n.1299+173_1299+180del
ENST00000405164.5:c.1323+173_1323+180del	ENSP00000384101.1:n.1323+173_1323+180del
ENST00000407946.5:c.*110_*117del	ENSP00000384552.1:n.*110_*117del
ENST00000465913.1:n.1020_1027del
ENST00000492082.5:n.1841+173_1841+180del
NM_000509.4:c.1299+173_1299+180del	NP_000500.2:n.1299+173_1299+180del
NM_000509.5:c.1299+173_1299+180del	NP_000500.2:n.1299+173_1299+180del
NM_021870.2:c.*110_*117del	NP_068656.2:n.*110_*117del
NM_021870.3:c.*110_*117del MANE Select	NP_068656.2:n.*110_*117del
NM_000509.6:c.1299+173_1299+180del	NP_000500.2:n.1299+173_1299+180del