Canonical Allele Identifier: CA1504935751

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569993_154569995delinsTAG , CM000666.2:g.154569993_154569995delinsTAG	GRCh38
NC_000004.11:g.155491145_155491147delinsTAG , CM000666.1:g.155491145_155491147delinsTAG	GRCh37
NC_000004.10:g.155710595_155710597delinsTAG	NCBI36
NG_008833.1:g.12014_12016delinsTAG , LRG_558:g.12014_12016delinsTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244+194_1244+196delinsTAG MANE Select	ENSP00000306099.4:n.1244+194_1244+196delinsTAG
ENST00000302068.8:c.1244+194_1244+196delinsTAG	ENSP00000306099.4:n.1244+194_1244+196delinsTAG
ENST00000502545.5:n.940-426_940-424delinsTAG
ENST00000509493.1:c.587+194_587+196delinsTAG	ENSP00000426757.1:n.587+194_587+196delinsTAG
NM_001184741.1:c.1067+194_1067+196delinsTAG	NP_001171670.1:n.1067+194_1067+196delinsTAG
NM_005141.4:c.1244+194_1244+196delinsTAG , LRG_558t1:c.1244+194_1244+196delinsTAG	NP_005132.2:n.1244+194_1244+196delinsTAG
NM_001382759.1:c.1112+194_1112+196delinsTAG	NP_001369688.1:n.1112+194_1112+196delinsTAG
NM_001382760.1:c.1244+194_1244+196delinsTAG	NP_001369689.1:n.1244+194_1244+196delinsTAG
NM_001382761.1:c.1244+194_1244+196delinsTAG	NP_001369690.1:n.1244+194_1244+196delinsTAG
NM_001382762.1:c.944+194_944+196delinsTAG	NP_001369691.1:n.944+194_944+196delinsTAG
NM_001382763.1:c.1235+194_1235+196delinsTAG	NP_001369692.1:n.1235+194_1235+196delinsTAG
NM_001382764.1:c.*18+194_*18+196delinsTAG	NP_001369693.1:n.*18+194_*18+196delinsTAG
NM_001382765.1:c.1220+218_1220+220delinsTAG	NP_001369694.1:n.1220+218_1220+220delinsTAG
NM_005141.5:c.1244+194_1244+196delinsTAG MANE Select	NP_005132.2:n.1244+194_1244+196delinsTAG