Canonical Allele Identifier: CA2672444869

Gene: FGG

Linked Data

• gnomAD v4: 4-154604818-G-GTTCTATAA

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154604820_154604821insCTATAATT , CM000666.2:g.154604820_154604821insCTATAATT	GRCh38
NC_000004.11:g.155525972_155525973insCTATAATT , CM000666.1:g.155525972_155525973insCTATAATT	GRCh37
NC_000004.10:g.155745422_155745423insCTATAATT	NCBI36
NG_008834.1:g.12932_12933insTTATAGAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.*15_*16insTTATAGAA MANE Select	ENSP00000336829.3:n.*15_*16insTTATAGAA
ENST00000336098.7:c.*15_*16insTTATAGAA	ENSP00000336829.3:n.*15_*16insTTATAGAA
ENST00000404648.7:c.1299+78_1299+79insTTATAGAA	ENSP00000384860.3:n.1299+78_1299+79insTTATAGAA
ENST00000405164.5:c.1323+78_1323+79insTTATAGAA	ENSP00000384101.1:n.1323+78_1323+79insTTATAGAA
ENST00000407946.5:c.*15_*16insTTATAGAA	ENSP00000384552.1:n.*15_*16insTTATAGAA
ENST00000465913.1:n.925_926insTTATAGAA
ENST00000492082.5:n.1841+78_1841+79insTTATAGAA
NM_000509.4:c.1299+78_1299+79insTTATAGAA	NP_000500.2:n.1299+78_1299+79insTTATAGAA
NM_000509.5:c.1299+78_1299+79insTTATAGAA	NP_000500.2:n.1299+78_1299+79insTTATAGAA
NM_021870.2:c.*15_*16insTTATAGAA	NP_068656.2:n.*15_*16insTTATAGAA
NM_021870.3:c.*15_*16insTTATAGAA MANE Select	NP_068656.2:n.*15_*16insTTATAGAA
NM_000509.6:c.1299+78_1299+79insTTATAGAA	NP_000500.2:n.1299+78_1299+79insTTATAGAA