Canonical Allele Identifier: CA196571797

Gene: FBP1

Linked Data

• dbSNP Id: rs891743971
• gnomAD v3: 9-94638817-C-CCCA
• gnomAD v4: 9-94638817-C-CCCA
• MyVariant Identifiers: chr9:g.97401099_97401100insCCA (hg19) ; chr9:g.94638817_94638818insCCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94638819_94638821dup , CM000671.2:g.94638819_94638821dup	GRCh38
NC_000009.11:g.97401101_97401103dup , CM000671.1:g.97401101_97401103dup	GRCh37
NC_000009.10:g.96440922_96440924dup	NCBI36
NG_008174.1:g.6430_6432dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+321_170+323dup	ENSP00000507547.1:n.170+321_170+323dup
ENST00000375326.9:c.170+321_170+323dup MANE Select	ENSP00000364475.5:n.170+321_170+323dup
ENST00000375326.8:c.170+321_170+323dup	ENSP00000364475.4:n.170+321_170+323dup
ENST00000414122.1:c.-83+1224_-83+1226dup	ENSP00000411619.1:n.-83+1224_-83+1226dup
ENST00000415431.5:c.170+321_170+323dup	ENSP00000408025.1:n.170+321_170+323dup
NM_000507.3:c.170+321_170+323dup	NP_000498.2:n.170+321_170+323dup
NM_001127628.1:c.170+321_170+323dup	NP_001121100.1:n.170+321_170+323dup
XM_006717005.2:c.-77+1224_-77+1226dup	XP_006717068.1:n.-77+1224_-77+1226dup
XM_006717005.4:c.-77+1224_-77+1226dup	XP_006717068.1:n.-77+1224_-77+1226dup
NM_000507.4:c.170+321_170+323dup MANE Select	NP_000498.2:n.170+321_170+323dup
NM_001127628.2:c.170+321_170+323dup	NP_001121100.1:n.170+321_170+323dup