Canonical Allele Identifier: CA915940559

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569796del , CM000666.2:g.154569796del	GRCh38
NC_000004.11:g.155490948del , CM000666.1:g.155490948del	GRCh37
NC_000004.10:g.155710398del	NCBI36
NG_008833.1:g.11817del , LRG_558:g.11817del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1241del MANE Select	ENSP00000306099.4:p.Gly414AlafsTer3
ENST00000302068.8:c.1241del	ENSP00000306099.4:p.Gly414AlafsTer3
ENST00000502545.5:n.939+489del
ENST00000509493.1:c.584del	ENSP00000426757.1:p.Gly195AlafsTer3
NM_001184741.1:c.1064del	NP_001171670.1:p.Gly355AlafsTer3
NM_005141.4:c.1241del , LRG_558t1:c.1241del	NP_005132.2:p.Gly414AlafsTer3
NM_001382759.1:c.1109del	NP_001369688.1:p.Gly370AlafsTer3
NM_001382760.1:c.1241del	NP_001369689.1:p.Gly414AlafsTer3
NM_001382761.1:c.1241del	NP_001369690.1:p.Gly414AlafsTer22
NM_001382762.1:c.941del	NP_001369691.1:p.Gly314AlafsTer3
NM_001382763.1:c.1232del	NP_001369692.1:p.Gly411AlafsTer3
NM_001382764.1:c.*15del	NP_001369693.1:n.*15del
NM_001382765.1:c.1220+21del	NP_001369694.1:n.1220+21del
NM_005141.5:c.1241del MANE Select	NP_005132.2:p.Gly414AlafsTer3