Canonical Allele Identifier: CA1504935657

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569798_154569799delinsTG , CM000666.2:g.154569798_154569799delinsTG	GRCh38
NC_000004.11:g.155490950_155490951delinsTG , CM000666.1:g.155490950_155490951delinsTG	GRCh37
NC_000004.10:g.155710400_155710401delinsTG	NCBI36
NG_008833.1:g.11819_11820delinsTG , LRG_558:g.11819_11820delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1243_1244delinsTG MANE Select	ENSP00000306099.4:p.Trp415=
ENST00000302068.8:c.1243_1244delinsTG	ENSP00000306099.4:p.Trp415=
ENST00000502545.5:n.939+491_939+492delinsTG
ENST00000509493.1:c.586_587delinsTG	ENSP00000426757.1:p.Trp196=
NM_001184741.1:c.1066_1067delinsTG	NP_001171670.1:p.Trp356=
NM_005141.4:c.1243_1244delinsTG , LRG_558t1:c.1243_1244delinsTG	NP_005132.2:p.Trp415=
NM_001382759.1:c.1111_1112delinsTG	NP_001369688.1:p.Trp371=
NM_001382760.1:c.1243_1244delinsTG	NP_001369689.1:p.Cys415=
NM_001382761.1:c.1243_1244delinsTG	NP_001369690.1:p.Ter415=
NM_001382762.1:c.943_944delinsTG	NP_001369691.1:p.Trp315=
NM_001382763.1:c.1234_1235delinsTG	NP_001369692.1:p.Trp412=
NM_001382764.1:c.*17_*18delinsTG	NP_001369693.1:n.*17_*18delinsTG
NM_001382765.1:c.1220+23_1220+24delinsTG	NP_001369694.1:n.1220+23_1220+24delinsTG
NM_005141.5:c.1243_1244delinsTG MANE Select	NP_005132.2:p.Trp415=