Canonical Allele Identifier: CA374106671

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97369124C>A (hg19) ; chr9:g.94606842C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94606842C>A , CM000671.2:g.94606842C>A	GRCh38
NC_000009.11:g.97369124C>A , CM000671.1:g.97369124C>A	GRCh37
NC_000009.10:g.96408945C>A	NCBI36
NG_008174.1:g.38408G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.838G>T	ENSP00000507547.1:n.838G>T
ENST00000375326.9:c.678G>T MANE Select	ENSP00000364475.5:p.Glu226Asp
ENST00000648117.1:c.483G>T	ENSP00000498145.1:p.Glu161Asp
ENST00000375326.8:c.678G>T	ENSP00000364475.4:p.Glu226Asp
ENST00000414122.1:c.426G>T	ENSP00000411619.1:p.Glu142Asp
ENST00000415431.5:c.678G>T	ENSP00000408025.1:p.Glu226Asp
NM_000507.3:c.678G>T	NP_000498.2:p.Glu226Asp
NM_001127628.1:c.678G>T	NP_001121100.1:p.Glu226Asp
XM_006717005.2:c.432G>T	XP_006717068.1:p.Glu144Asp
XM_006717005.4:c.432G>T	XP_006717068.1:p.Glu144Asp
NM_000507.4:c.678G>T MANE Select	NP_000498.2:p.Glu226Asp
NM_001127628.2:c.678G>T	NP_001121100.1:p.Glu226Asp