Canonical Allele Identifier: CA374107606

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97372207T>G (hg19) ; chr9:g.94609925T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94609925T>G , CM000671.2:g.94609925T>G	GRCh38
NC_000009.11:g.97372207T>G , CM000671.1:g.97372207T>G	GRCh37
NC_000009.10:g.96412028T>G	NCBI36
NG_008174.1:g.35325A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.563A>C	ENSP00000507547.1:p.Asp188Ala
ENST00000375326.9:c.563A>C MANE Select	ENSP00000364475.5:p.Asp188Ala
ENST00000648117.1:c.368A>C	ENSP00000498145.1:p.Asp123Ala
ENST00000375326.8:c.563A>C	ENSP00000364475.4:p.Asp188Ala
ENST00000414122.1:c.311A>C	ENSP00000411619.1:p.Asp104Ala
ENST00000415431.5:c.563A>C	ENSP00000408025.1:p.Asp188Ala
NM_000507.3:c.563A>C	NP_000498.2:p.Asp188Ala
NM_001127628.1:c.563A>C	NP_001121100.1:p.Asp188Ala
XM_006717005.2:c.317A>C	XP_006717068.1:p.Asp106Ala
XM_006717005.4:c.317A>C	XP_006717068.1:p.Asp106Ala
NM_000507.4:c.563A>C MANE Select	NP_000498.2:p.Asp188Ala
NM_001127628.2:c.563A>C	NP_001121100.1:p.Asp188Ala