Canonical Allele Identifier: CA2672444880

Gene: FGG

Linked Data

• gnomAD v4: 4-154604973-G-GT

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604977dup , CM000666.2:g.154604977dup	GRCh38
NC_000004.11:g.155526129dup , CM000666.1:g.155526129dup	GRCh37
NC_000004.10:g.155745579dup	NCBI36
NG_008834.1:g.12777dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1222dup MANE Select	ENSP00000336829.3:p.Thr408AsnfsTer?
ENST00000336098.7:c.1222dup	ENSP00000336829.3:p.Thr408AsnfsTer?
ENST00000404648.7:c.1222dup	ENSP00000384860.3:p.Thr408AsnfsTer?
ENST00000405164.5:c.1246dup	ENSP00000384101.1:p.Thr416AsnfsTer?
ENST00000407946.5:c.1246dup	ENSP00000384552.1:p.Thr416AsnfsTer?
ENST00000465913.1:n.770dup
ENST00000492082.5:n.1764dup
NM_000509.4:c.1222dup	NP_000500.2:p.Thr408AsnfsTer?
NM_000509.5:c.1222dup	NP_000500.2:p.Thr408AsnfsTer?
NM_021870.2:c.1222dup	NP_068656.2:p.Thr408AsnfsTer?
NM_021870.3:c.1222dup MANE Select	NP_068656.2:p.Thr408AsnfsTer?
NM_000509.6:c.1222dup	NP_000500.2:p.Thr408AsnfsTer?