Canonical Allele Identifier: CA1069726143

Gene: FGG

Linked Data

• dbSNP Id: rs1731067488
• gnomAD v3: 4-154604829-A-AT
• gnomAD v4: 4-154604829-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604833dup , CM000666.2:g.154604833dup	GRCh38
NC_000004.11:g.155525985dup , CM000666.1:g.155525985dup	GRCh37
NC_000004.10:g.155745435dup	NCBI36
NG_008834.1:g.12921dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000336098.8:c.*4dup MANE Select	ENSP00000336829.3:n.*4dup
ENST00000336098.7:c.*4dup	ENSP00000336829.3:n.*4dup
ENST00000404648.7:c.1299+67dup	ENSP00000384860.3:n.1299+67dup
ENST00000405164.5:c.1323+67dup	ENSP00000384101.1:n.1323+67dup
ENST00000407946.5:c.*4dup	ENSP00000384552.1:n.*4dup
ENST00000465913.1:n.914dup
ENST00000492082.5:n.1841+67dup
NM_000509.4:c.1299+67dup	NP_000500.2:n.1299+67dup
NM_000509.5:c.1299+67dup	NP_000500.2:n.1299+67dup
NM_021870.2:c.*4dup	NP_068656.2:n.*4dup
NM_021870.3:c.*4dup MANE Select	NP_068656.2:n.*4dup
NM_000509.6:c.1299+67dup	NP_000500.2:n.1299+67dup