Canonical Allele Identifier: CA1865264885

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94638998_94639002delinsCAGAG , CM000671.2:g.94638998_94639002delinsCAGAG	GRCh38
NC_000009.11:g.97401280_97401284delinsCAGAG , CM000671.1:g.97401280_97401284delinsCAGAG	GRCh37
NC_000009.10:g.96441101_96441105delinsCAGAG	NCBI36
NG_008174.1:g.6248_6252delinsCTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+139_170+143delinsCTCTG	ENSP00000507547.1:n.170+139_170+143delinsCTCTG
ENST00000375326.9:c.170+139_170+143delinsCTCTG MANE Select	ENSP00000364475.5:n.170+139_170+143delinsCTCTG
ENST00000375326.8:c.170+139_170+143delinsCTCTG	ENSP00000364475.4:n.170+139_170+143delinsCTCTG
ENST00000414122.1:c.-83+1042_-83+1046delinsCTCTG	ENSP00000411619.1:n.-83+1042_-83+1046delinsCTCTG
ENST00000415431.5:c.170+139_170+143delinsCTCTG	ENSP00000408025.1:n.170+139_170+143delinsCTCTG
NM_000507.3:c.170+139_170+143delinsCTCTG	NP_000498.2:n.170+139_170+143delinsCTCTG
NM_001127628.1:c.170+139_170+143delinsCTCTG	NP_001121100.1:n.170+139_170+143delinsCTCTG
XM_006717005.2:c.-77+1042_-77+1046delinsCTCTG	XP_006717068.1:n.-77+1042_-77+1046delinsCTCTG
XM_006717005.4:c.-77+1042_-77+1046delinsCTCTG	XP_006717068.1:n.-77+1042_-77+1046delinsCTCTG
NM_000507.4:c.170+139_170+143delinsCTCTG MANE Select	NP_000498.2:n.170+139_170+143delinsCTCTG
NM_001127628.2:c.170+139_170+143delinsCTCTG	NP_001121100.1:n.170+139_170+143delinsCTCTG