Canonical Allele Identifier: CA1504935670

Gene: FGB

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.154569814_154569816delinsCTT , CM000666.2:g.154569814_154569816delinsCTT	GRCh38
NC_000004.11:g.155490966_155490968delinsCTT , CM000666.1:g.155490966_155490968delinsCTT	GRCh37
NC_000004.10:g.155710416_155710418delinsCTT	NCBI36
NG_008833.1:g.11835_11837delinsCTT , LRG_558:g.11835_11837delinsCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302068.9:c.1244+15_1244+17delinsCTT MANE Select	ENSP00000306099.4:n.1244+15_1244+17delinsCTT
ENST00000302068.8:c.1244+15_1244+17delinsCTT	ENSP00000306099.4:n.1244+15_1244+17delinsCTT
ENST00000502545.5:n.939+507_939+509delinsCTT
ENST00000509493.1:c.587+15_587+17delinsCTT	ENSP00000426757.1:n.587+15_587+17delinsCTT
NM_001184741.1:c.1067+15_1067+17delinsCTT	NP_001171670.1:n.1067+15_1067+17delinsCTT
NM_005141.4:c.1244+15_1244+17delinsCTT , LRG_558t1:c.1244+15_1244+17delinsCTT	NP_005132.2:n.1244+15_1244+17delinsCTT
NM_001382759.1:c.1112+15_1112+17delinsCTT	NP_001369688.1:n.1112+15_1112+17delinsCTT
NM_001382760.1:c.1244+15_1244+17delinsCTT	NP_001369689.1:n.1244+15_1244+17delinsCTT
NM_001382761.1:c.1244+15_1244+17delinsCTT	NP_001369690.1:n.1244+15_1244+17delinsCTT
NM_001382762.1:c.944+15_944+17delinsCTT	NP_001369691.1:n.944+15_944+17delinsCTT
NM_001382763.1:c.1235+15_1235+17delinsCTT	NP_001369692.1:n.1235+15_1235+17delinsCTT
NM_001382764.1:c.*18+15_*18+17delinsCTT	NP_001369693.1:n.*18+15_*18+17delinsCTT
NM_001382765.1:c.1220+39_1220+41delinsCTT	NP_001369694.1:n.1220+39_1220+41delinsCTT
NM_005141.5:c.1244+15_1244+17delinsCTT MANE Select	NP_005132.2:n.1244+15_1244+17delinsCTT