Canonical Allele Identifier: CA374335014

Gene: FBP1

Linked Data

• gnomAD v4: 9-94639156-G-A
• MyVariant Identifiers: chr9:g.97401438G>A (hg19) ; chr9:g.94639156G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94639156G>A , CM000671.2:g.94639156G>A	GRCh38
NC_000009.11:g.97401438G>A , CM000671.1:g.97401438G>A	GRCh37
NC_000009.10:g.96441259G>A	NCBI36
NG_008174.1:g.6094C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.155C>T	ENSP00000507547.1:p.Ala52Val
ENST00000375326.9:c.155C>T MANE Select	ENSP00000364475.5:p.Ala52Val
ENST00000375326.8:c.155C>T	ENSP00000364475.4:p.Ala52Val
ENST00000414122.1:c.-83+888C>T	ENSP00000411619.1:n.-83+888C>T
ENST00000415431.5:c.155C>T	ENSP00000408025.1:p.Ala52Val
NM_000507.3:c.155C>T	NP_000498.2:p.Ala52Val
NM_001127628.1:c.155C>T	NP_001121100.1:p.Ala52Val
XM_006717005.2:c.-77+888C>T	XP_006717068.1:n.-77+888C>T
XM_006717005.4:c.-77+888C>T	XP_006717068.1:n.-77+888C>T
NM_000507.4:c.155C>T MANE Select	NP_000498.2:p.Ala52Val
NM_001127628.2:c.155C>T	NP_001121100.1:p.Ala52Val