Canonical Allele Identifier: CA645540053

Gene: FGB

Linked Data

• COSMIC: COSM311169

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569759_154569760delinsTT , CM000666.2:g.154569759_154569760delinsTT	GRCh38
NC_000004.11:g.155490911_155490912delinsTT , CM000666.1:g.155490911_155490912delinsTT	GRCh37
NC_000004.10:g.155710361_155710362delinsTT	NCBI36
NG_008833.1:g.11780_11781delinsTT , LRG_558:g.11780_11781delinsTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1204_1205delinsTT MANE Select	ENSP00000306099.4:p.Gly402Phe
ENST00000302068.8:c.1204_1205delinsTT	ENSP00000306099.4:p.Gly402Phe
ENST00000502545.5:n.939+452_939+453delinsTT
ENST00000509493.1:c.547_548delinsTT	ENSP00000426757.1:p.Gly183Phe
NM_001184741.1:c.1027_1028delinsTT	NP_001171670.1:p.Gly343Phe
NM_005141.4:c.1204_1205delinsTT , LRG_558t1:c.1204_1205delinsTT	NP_005132.2:p.Gly402Phe
NM_001382759.1:c.1072_1073delinsTT	NP_001369688.1:p.Gly358Phe
NM_001382760.1:c.1204_1205delinsTT	NP_001369689.1:p.Gly402Phe
NM_001382761.1:c.1204_1205delinsTT	NP_001369690.1:p.Gly402Phe
NM_001382762.1:c.904_905delinsTT	NP_001369691.1:p.Gly302Phe
NM_001382763.1:c.1195_1196delinsTT	NP_001369692.1:p.Gly399Phe
NM_001382764.1:c.1081-14_1081-13delinsTT	NP_001369693.1:n.1081-14_1081-13delinsTT
NM_001382765.1:c.1204_1205delinsTT	NP_001369694.1:p.Gly402Phe
NM_005141.5:c.1204_1205delinsTT MANE Select	NP_005132.2:p.Gly402Phe