Canonical Allele Identifier: CA374106681

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97369126C>G (hg19) ; chr9:g.94606844C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94606844C>G , CM000671.2:g.94606844C>G	GRCh38
NC_000009.11:g.97369126C>G , CM000671.1:g.97369126C>G	GRCh37
NC_000009.10:g.96408947C>G	NCBI36
NG_008174.1:g.38406G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.836G>C	ENSP00000507547.1:n.836G>C
ENST00000375326.9:c.676G>C MANE Select	ENSP00000364475.5:p.Glu226Gln
ENST00000648117.1:c.481G>C	ENSP00000498145.1:p.Glu161Gln
ENST00000375326.8:c.676G>C	ENSP00000364475.4:p.Glu226Gln
ENST00000414122.1:c.424G>C	ENSP00000411619.1:p.Glu142Gln
ENST00000415431.5:c.676G>C	ENSP00000408025.1:p.Glu226Gln
NM_000507.3:c.676G>C	NP_000498.2:p.Glu226Gln
NM_001127628.1:c.676G>C	NP_001121100.1:p.Glu226Gln
XM_006717005.2:c.430G>C	XP_006717068.1:p.Glu144Gln
XM_006717005.4:c.430G>C	XP_006717068.1:p.Glu144Gln
NM_000507.4:c.676G>C MANE Select	NP_000498.2:p.Glu226Gln
NM_001127628.2:c.676G>C	NP_001121100.1:p.Glu226Gln