Canonical Allele Identifier: CA2695210729

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639196_94639197insTGCAG , CM000671.2:g.94639196_94639197insTGCAG	GRCh38
NC_000009.11:g.97401478_97401479insTGCAG , CM000671.1:g.97401478_97401479insTGCAG	GRCh37
NC_000009.10:g.96441299_96441300insTGCAG	NCBI36
NG_008174.1:g.6053_6054insCTGCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.114_115insCTGCA	ENSP00000507547.1:p.Cys39LeufsTer30
ENST00000375326.9:c.114_115insCTGCA MANE Select	ENSP00000364475.5:p.Cys39LeufsTer30
ENST00000375326.8:c.114_115insCTGCA	ENSP00000364475.4:p.Cys39LeufsTer30
ENST00000414122.1:c.-83+847_-83+848insCTGCA	ENSP00000411619.1:n.-83+847_-83+848insCTGCA
ENST00000415431.5:c.114_115insCTGCA	ENSP00000408025.1:p.Cys39LeufsTer30
NM_000507.3:c.114_115insCTGCA	NP_000498.2:p.Cys39LeufsTer30
NM_001127628.1:c.114_115insCTGCA	NP_001121100.1:p.Cys39LeufsTer30
XM_006717005.2:c.-77+847_-77+848insCTGCA	XP_006717068.1:n.-77+847_-77+848insCTGCA
XM_006717005.4:c.-77+847_-77+848insCTGCA	XP_006717068.1:n.-77+847_-77+848insCTGCA
NM_000507.4:c.114_115insCTGCA MANE Select	NP_000498.2:p.Cys39LeufsTer30
NM_001127628.2:c.114_115insCTGCA	NP_001121100.1:p.Cys39LeufsTer30