Canonical Allele Identifier: CA1865265243

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639262_94639263delinsAG , CM000671.2:g.94639262_94639263delinsAG	GRCh38
NC_000009.11:g.97401544_97401545delinsAG , CM000671.1:g.97401544_97401545delinsAG	GRCh37
NC_000009.10:g.96441365_96441366delinsAG	NCBI36
NG_008174.1:g.5987_5988delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.48_49delinsCT	ENSP00000507547.1:p.Arg16=
ENST00000375326.9:c.48_49delinsCT MANE Select	ENSP00000364475.5:p.Arg16=
ENST00000375326.8:c.48_49delinsCT	ENSP00000364475.4:p.Arg16=
ENST00000414122.1:c.-83+781_-83+782delinsCT	ENSP00000411619.1:n.-83+781_-83+782delinsCT
ENST00000415431.5:c.48_49delinsCT	ENSP00000408025.1:p.Arg16=
NM_000507.3:c.48_49delinsCT	NP_000498.2:p.Arg16=
NM_001127628.1:c.48_49delinsCT	NP_001121100.1:p.Arg16=
XM_006717005.2:c.-77+781_-77+782delinsCT	XP_006717068.1:n.-77+781_-77+782delinsCT
XM_006717005.4:c.-77+781_-77+782delinsCT	XP_006717068.1:n.-77+781_-77+782delinsCT
NM_000507.4:c.48_49delinsCT MANE Select	NP_000498.2:p.Arg16=
NM_001127628.2:c.48_49delinsCT	NP_001121100.1:p.Arg16=