Canonical Allele Identifier: CA789378563

Gene: FGG

Linked Data

• dbSNP Id: rs1257903220
• gnomAD v4: 4-154604764-A-AG
• MyVariant Identifiers: chr4:g.155525916_155525917insG (hg19) ; chr4:g.154604764_154604765insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604765dup , CM000666.2:g.154604765dup	GRCh38
NC_000004.11:g.155525917dup , CM000666.1:g.155525917dup	GRCh37
NC_000004.10:g.155745367dup	NCBI36
NG_008834.1:g.12986dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.*69dup MANE Select	ENSP00000336829.3:n.*69dup
ENST00000336098.7:c.*69dup	ENSP00000336829.3:n.*69dup
ENST00000404648.7:c.1299+132dup	ENSP00000384860.3:n.1299+132dup
ENST00000405164.5:c.1323+132dup	ENSP00000384101.1:n.1323+132dup
ENST00000407946.5:c.*69dup	ENSP00000384552.1:n.*69dup
ENST00000465913.1:n.979dup
ENST00000492082.5:n.1841+132dup
NM_000509.4:c.1299+132dup	NP_000500.2:n.1299+132dup
NM_000509.5:c.1299+132dup	NP_000500.2:n.1299+132dup
NM_021870.2:c.*69dup	NP_068656.2:n.*69dup
NM_021870.3:c.*69dup MANE Select	NP_068656.2:n.*69dup
NM_000509.6:c.1299+132dup	NP_000500.2:n.1299+132dup