Canonical Allele Identifier: CA2695204008

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154565811_154565817dup , CM000666.2:g.154565811_154565817dup	GRCh38
NC_000004.11:g.155486963_155486969dup , CM000666.1:g.155486963_155486969dup	GRCh37
NC_000004.10:g.155706413_155706419dup	NCBI36
NG_008833.1:g.7832_7838dup , LRG_558:g.7832_7838dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000302068.9:c.118_124dup MANE Select	ENSP00000306099.4:p.Ser42IlefsTer11
ENST00000302068.8:c.118_124dup	ENSP00000306099.4:p.Ser42IlefsTer11
ENST00000425838.5:c.*30_*36dup	ENSP00000398719.1:n.*30_*36dup
ENST00000473984.1:n.31_37dup
ENST00000497097.5:n.125_131dup
ENST00000498375.2:n.748_754dup
ENST00000502545.5:n.99_105dup
ENST00000509493.1:c.-167-1782_-167-1776dup	ENSP00000426757.1:n.-167-1782_-167-1776du...
NM_001184741.1:c.118_124dup	NP_001171670.1:p.Ser42IlefsTer11
NM_005141.4:c.118_124dup , LRG_558t1:c.118_124dup	NP_005132.2:p.Ser42IlefsTer11
NM_001382759.1:c.118_124dup	NP_001369688.1:p.Ser42IlefsTer11
NM_001382760.1:c.118_124dup	NP_001369689.1:p.Ser42IlefsTer11
NM_001382761.1:c.118_124dup	NP_001369690.1:p.Ser42IlefsTer11
NM_001382762.1:c.118_124dup	NP_001369691.1:p.Ser42IlefsTer11
NM_001382763.1:c.118_124dup	NP_001369692.1:p.Ser42IlefsTer11
NM_001382764.1:c.118_124dup	NP_001369693.1:p.Ser42IlefsTer11
NM_001382765.1:c.118_124dup	NP_001369694.1:p.Ser42IlefsTer11
NM_005141.5:c.118_124dup MANE Select	NP_005132.2:p.Ser42IlefsTer11