Canonical Allele Identifier: CA2672444896

Gene: FGG

Linked Data

• gnomAD v4: 4-154605132-GAGCTGTCTATTACGAAGTGCAT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154605133_154605154del , CM000666.2:g.154605133_154605154del	GRCh38
NC_000004.11:g.155526285_155526306del , CM000666.1:g.155526285_155526306del	GRCh37
NC_000004.10:g.155745735_155745756del	NCBI36
NG_008834.1:g.12597_12618del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000336098.8:c.1130-88_1130-67del MANE Select	ENSP00000336829.3:n.1130-88_1130-67del
ENST00000336098.7:c.1130-88_1130-67del	ENSP00000336829.3:n.1130-88_1130-67del
ENST00000404648.7:c.1130-88_1130-67del	ENSP00000384860.3:n.1130-88_1130-67del
ENST00000405164.5:c.1154-88_1154-67del	ENSP00000384101.1:n.1154-88_1154-67del
ENST00000407946.5:c.1154-88_1154-67del	ENSP00000384552.1:n.1154-88_1154-67del
ENST00000465913.1:n.678-88_678-67del
ENST00000492082.5:n.1672-88_1672-67del
NM_000509.4:c.1130-88_1130-67del	NP_000500.2:n.1130-88_1130-67del
NM_000509.5:c.1130-88_1130-67del	NP_000500.2:n.1130-88_1130-67del
NM_021870.2:c.1130-88_1130-67del	NP_068656.2:n.1130-88_1130-67del
NM_021870.3:c.1130-88_1130-67del MANE Select	NP_068656.2:n.1130-88_1130-67del
NM_000509.6:c.1130-88_1130-67del	NP_000500.2:n.1130-88_1130-67del