Canonical Allele Identifier: CA2672441406

Gene: FGB

Linked Data

• gnomAD v4: 4-154569667-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569668_154569669del , CM000666.2:g.154569668_154569669del	GRCh38
NC_000004.11:g.155490820_155490821del , CM000666.1:g.155490820_155490821del	GRCh37
NC_000004.10:g.155710270_155710271del	NCBI36
NG_008833.1:g.11689_11690del , LRG_558:g.11689_11690del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1113_1114del MANE Select	ENSP00000306099.4:p.Val372GlufsTer9
ENST00000302068.8:c.1113_1114del	ENSP00000306099.4:p.Val372GlufsTer9
ENST00000502545.5:n.939+361_939+362del
ENST00000509493.1:c.456_457del	ENSP00000426757.1:p.Val153GlufsTer9
NM_001184741.1:c.936_937del	NP_001171670.1:p.Val313GlufsTer9
NM_005141.4:c.1113_1114del , LRG_558t1:c.1113_1114del	NP_005132.2:p.Val372GlufsTer9
NM_001382759.1:c.981_982del	NP_001369688.1:p.Val328GlufsTer9
NM_001382760.1:c.1113_1114del	NP_001369689.1:p.Val372GlufsTer9
NM_001382761.1:c.1113_1114del	NP_001369690.1:p.Val372GlufsTer9
NM_001382762.1:c.813_814del	NP_001369691.1:p.Val272GlufsTer9
NM_001382763.1:c.1104_1105del	NP_001369692.1:p.Val369GlufsTer9
NM_001382764.1:c.1080+33_1080+34del	NP_001369693.1:n.1080+33_1080+34del
NM_001382765.1:c.1113_1114del	NP_001369694.1:p.Val372GlufsTer9
NM_005141.5:c.1113_1114del MANE Select	NP_005132.2:p.Val372GlufsTer9