Canonical Allele Identifier: CA555971688

Gene: FGG

Linked Data

• dbSNP Id: rs1339869472
• gnomAD v2: 4-155525905-A-AAT
• gnomAD v3: 4-154604753-A-AAT
• gnomAD v4: 4-154604753-A-AAT
• MyVariant Identifiers: chr4:g.155525905_155525906insAT (hg19) ; chr4:g.154604753_154604754insAT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604757_154604758dup , CM000666.2:g.154604757_154604758dup	GRCh38
NC_000004.11:g.155525909_155525910dup , CM000666.1:g.155525909_155525910dup	GRCh37
NC_000004.10:g.155745359_155745360dup	NCBI36
NG_008834.1:g.12996_12997dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000336098.8:c.*79_*80dup MANE Select	ENSP00000336829.3:n.*79_*80dup
ENST00000336098.7:c.*79_*80dup	ENSP00000336829.3:n.*79_*80dup
ENST00000404648.7:c.1299+142_1299+143dup	ENSP00000384860.3:n.1299+142_1299+143dup
ENST00000405164.5:c.1323+142_1323+143dup	ENSP00000384101.1:n.1323+142_1323+143dup
ENST00000407946.5:c.*79_*80dup	ENSP00000384552.1:n.*79_*80dup
ENST00000465913.1:n.989_990dup
ENST00000492082.5:n.1841+142_1841+143dup
NM_000509.4:c.1299+142_1299+143dup	NP_000500.2:n.1299+142_1299+143dup
NM_000509.5:c.1299+142_1299+143dup	NP_000500.2:n.1299+142_1299+143dup
NM_021870.2:c.*79_*80dup	NP_068656.2:n.*79_*80dup
NM_021870.3:c.*79_*80dup MANE Select	NP_068656.2:n.*79_*80dup
NM_000509.6:c.1299+142_1299+143dup	NP_000500.2:n.1299+142_1299+143dup