Canonical Allele Identifier: CA868715188

Gene: FBP1

Linked Data

• dbSNP Id: rs1390311704
• gnomAD v3: 9-94638794-GGGTATGACGGGCA-G
• gnomAD v4: 9-94638794-GGGTATGACGGGCA-G
• MyVariant Identifiers: chr9:g.97401077_97401089del (hg19) ; chr9:g.94638795_94638807del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94638797_94638809del , CM000671.2:g.94638797_94638809del	GRCh38
NC_000009.11:g.97401079_97401091del , CM000671.1:g.97401079_97401091del	GRCh37
NC_000009.10:g.96440900_96440912del	NCBI36
NG_008174.1:g.6443_6455del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+334_170+346del	ENSP00000507547.1:n.170+334_170+346del
ENST00000375326.9:c.170+334_170+346del MANE Select	ENSP00000364475.5:n.170+334_170+346del
ENST00000375326.8:c.170+334_170+346del	ENSP00000364475.4:n.170+334_170+346del
ENST00000414122.1:c.-83+1237_-83+1249del	ENSP00000411619.1:n.-83+1237_-83+1249del
ENST00000415431.5:c.170+334_170+346del	ENSP00000408025.1:n.170+334_170+346del
NM_000507.3:c.170+334_170+346del	NP_000498.2:n.170+334_170+346del
NM_001127628.1:c.170+334_170+346del	NP_001121100.1:n.170+334_170+346del
XM_006717005.2:c.-77+1237_-77+1249del	XP_006717068.1:n.-77+1237_-77+1249del
XM_006717005.4:c.-77+1237_-77+1249del	XP_006717068.1:n.-77+1237_-77+1249del
NM_000507.4:c.170+334_170+346del MANE Select	NP_000498.2:n.170+334_170+346del
NM_001127628.2:c.170+334_170+346del	NP_001121100.1:n.170+334_170+346del