Canonical Allele Identifier: CA1865265088

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639166_94639174delinsCCGCCGAAG , CM000671.2:g.94639166_94639174delinsCCGCCGAAG	GRCh38
NC_000009.11:g.97401448_97401456delinsCCGCCGAAG , CM000671.1:g.97401448_97401456delinsCCGCCGAAG	GRCh37
NC_000009.10:g.96441269_96441277delinsCCGCCGAAG	NCBI36
NG_008174.1:g.6076_6084delinsCTTCGGCGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.137_145delinsCTTCGGCGG	ENSP00000507547.1:p.Ser46=
ENST00000375326.9:c.137_145delinsCTTCGGCGG MANE Select	ENSP00000364475.5:p.Ser46=
ENST00000375326.8:c.137_145delinsCTTCGGCGG	ENSP00000364475.4:p.Ser46=
ENST00000414122.1:c.-83+870_-83+878delinsCTTCGGCGG	ENSP00000411619.1:n.-83+870_-83+878delinsCTTCGGCGG
ENST00000415431.5:c.137_145delinsCTTCGGCGG	ENSP00000408025.1:p.Ser46=
NM_000507.3:c.137_145delinsCTTCGGCGG	NP_000498.2:p.Ser46=
NM_001127628.1:c.137_145delinsCTTCGGCGG	NP_001121100.1:p.Ser46=
XM_006717005.2:c.-77+870_-77+878delinsCTTCGGCGG	XP_006717068.1:n.-77+870_-77+878delinsCTTCGGCGG
XM_006717005.4:c.-77+870_-77+878delinsCTTCGGCGG	XP_006717068.1:n.-77+870_-77+878delinsCTTCGGCGG
NM_000507.4:c.137_145delinsCTTCGGCGG MANE Select	NP_000498.2:p.Ser46=
NM_001127628.2:c.137_145delinsCTTCGGCGG	NP_001121100.1:p.Ser46=