Canonical Allele Identifier: CA2840049753

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565884_154565885insTCCACTGATGGGCGGTGGGGCAG , CM000666.2:g.154565884_154565885insTCCACTGATGGGCGGTGGGGCAG	GRCh38
NC_000004.11:g.155487036_155487037insTCCACTGATGGGCGGTGGGGCAG , CM000666.1:g.155487036_155487037insTCCACTGATGGGCGGTGGGGCAG	GRCh37
NC_000004.10:g.155706486_155706487insTCCACTGATGGGCGGTGGGGCAG	NCBI36
NG_008833.1:g.7905_7906insTCCACTGATGGGCGGTGGGGCAG , LRG_558:g.7905_7906insTCCACTGATGGGCGGTGGGGCAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.191_192insTCCACTGATGGGCGGTGGGGCAG MANE Select	ENSP00000306099.4:p.Ile66LeufsTer28
ENST00000302068.8:c.191_192insTCCACTGATGGGCGGTGGGGCAG	ENSP00000306099.4:p.Ile66LeufsTer28
ENST00000425838.5:c.*103_*104insTCCACTGATGGGCGGTGGGGCAG	ENSP00000398719.1:n.*103_*104insTCCACTGATGGGCGGTGGGGCAG
ENST00000473984.1:n.104_105insTCCACTGATGGGCGGTGGGGCAG
ENST00000497097.5:n.198_199insTCCACTGATGGGCGGTGGGGCAG
ENST00000498375.2:n.821_822insTCCACTGATGGGCGGTGGGGCAG
ENST00000502545.5:n.172_173insTCCACTGATGGGCGGTGGGGCAG
ENST00000509493.1:c.-167-1709_-167-1708insTCCACTGATGGGCGGTGGGGCAG	ENSP00000426757.1:n.-167-1709_-167-1708insTCCACTGATGGGCGGTGGG...
NM_001184741.1:c.165+26_165+27insTCCACTGATGGGCGGTGGGGCAG	NP_001171670.1:n.165+26_165+27insTCCACTGATGGGCGGTGGGGCAG
NM_005141.4:c.191_192insTCCACTGATGGGCGGTGGGGCAG , LRG_558t1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_005132.2:p.Ile66LeufsTer28
NM_001382759.1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_001369688.1:p.Ile66LeufsTer28
NM_001382760.1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_001369689.1:p.Ile66LeufsTer28
NM_001382761.1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_001369690.1:p.Ile66LeufsTer28
NM_001382762.1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_001369691.1:p.Ile66LeufsTer28
NM_001382763.1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_001369692.1:p.Ile66LeufsTer28
NM_001382764.1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_001369693.1:p.Ile66LeufsTer28
NM_001382765.1:c.191_192insTCCACTGATGGGCGGTGGGGCAG	NP_001369694.1:p.Ile66LeufsTer28
NM_005141.5:c.191_192insTCCACTGATGGGCGGTGGGGCAG MANE Select	NP_005132.2:p.Ile66LeufsTer28