Canonical Allele Identifier: CA2840156961

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565890_154565891insGGG , CM000666.2:g.154565890_154565891insGGG	GRCh38
NC_000004.11:g.155487042_155487043insGGG , CM000666.1:g.155487042_155487043insGGG	GRCh37
NC_000004.10:g.155706492_155706493insGGG	NCBI36
NG_008833.1:g.7911_7912insGGG , LRG_558:g.7911_7912insGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.197_198insGGG MANE Select	ENSP00000306099.4:p.Ile66delinsMetGly
ENST00000302068.8:c.197_198insGGG	ENSP00000306099.4:p.Ile66delinsMetGly
ENST00000425838.5:c.*109_*110insGGG	ENSP00000398719.1:n.*109_*110insGGG
ENST00000473984.1:n.110_111insGGG
ENST00000497097.5:n.204_205insGGG
ENST00000498375.2:n.827_828insGGG
ENST00000502545.5:n.178_179insGGG
ENST00000509493.1:c.-167-1703_-167-1702insGGG	ENSP00000426757.1:n.-167-1703_-167-1702insGGG
NM_001184741.1:c.165+32_165+33insGGG	NP_001171670.1:n.165+32_165+33insGGG
NM_005141.4:c.197_198insGGG , LRG_558t1:c.197_198insGGG	NP_005132.2:p.Ile66delinsMetGly
NM_001382759.1:c.197_198insGGG	NP_001369688.1:p.Ile66delinsMetGly
NM_001382760.1:c.197_198insGGG	NP_001369689.1:p.Ile66delinsMetGly
NM_001382761.1:c.197_198insGGG	NP_001369690.1:p.Ile66delinsMetGly
NM_001382762.1:c.197_198insGGG	NP_001369691.1:p.Ile66delinsMetGly
NM_001382763.1:c.197_198insGGG	NP_001369692.1:p.Ile66delinsMetGly
NM_001382764.1:c.197_198insGGG	NP_001369693.1:p.Ile66delinsMetGly
NM_001382765.1:c.197_198insGGG	NP_001369694.1:p.Ile66delinsMetGly
NM_005141.5:c.197_198insGGG MANE Select	NP_005132.2:p.Ile66delinsMetGly