Canonical Allele Identifier: CA2690769888

Gene: FBP1

Linked Data

• gnomAD v4: 9-94639103-CAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639105_94639106del , CM000671.2:g.94639105_94639106del	GRCh38
NC_000009.11:g.97401387_97401388del , CM000671.1:g.97401387_97401388del	GRCh37
NC_000009.10:g.96441208_96441209del	NCBI36
NG_008174.1:g.6145_6146del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+36_170+37del	ENSP00000507547.1:n.170+36_170+37del
ENST00000375326.9:c.170+36_170+37del MANE Select	ENSP00000364475.5:n.170+36_170+37del
ENST00000375326.8:c.170+36_170+37del	ENSP00000364475.4:n.170+36_170+37del
ENST00000414122.1:c.-83+939_-83+940del	ENSP00000411619.1:n.-83+939_-83+940del
ENST00000415431.5:c.170+36_170+37del	ENSP00000408025.1:n.170+36_170+37del
NM_000507.3:c.170+36_170+37del	NP_000498.2:n.170+36_170+37del
NM_001127628.1:c.170+36_170+37del	NP_001121100.1:n.170+36_170+37del
XM_006717005.2:c.-77+939_-77+940del	XP_006717068.1:n.-77+939_-77+940del
XM_006717005.4:c.-77+939_-77+940del	XP_006717068.1:n.-77+939_-77+940del
NM_000507.4:c.170+36_170+37del MANE Select	NP_000498.2:n.170+36_170+37del
NM_001127628.2:c.170+36_170+37del	NP_001121100.1:n.170+36_170+37del