Canonical Allele Identifier: CA374106691

Gene: FBP1

Linked Data

• MyVariant Identifiers: chr9:g.97369129T>C (hg19) ; chr9:g.94606847T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94606847T>C , CM000671.2:g.94606847T>C	GRCh38
NC_000009.11:g.97369129T>C , CM000671.1:g.97369129T>C	GRCh37
NC_000009.10:g.96408950T>C	NCBI36
NG_008174.1:g.38403A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682520.1:c.833A>G	ENSP00000507547.1:n.833A>G
ENST00000375326.9:c.673A>G MANE Select	ENSP00000364475.5:p.Thr225Ala
ENST00000648117.1:c.478A>G	ENSP00000498145.1:p.Thr160Ala
ENST00000375326.8:c.673A>G	ENSP00000364475.4:p.Thr225Ala
ENST00000414122.1:c.421A>G	ENSP00000411619.1:p.Thr141Ala
ENST00000415431.5:c.673A>G	ENSP00000408025.1:p.Thr225Ala
NM_000507.3:c.673A>G	NP_000498.2:p.Thr225Ala
NM_001127628.1:c.673A>G	NP_001121100.1:p.Thr225Ala
XM_006717005.2:c.427A>G	XP_006717068.1:p.Thr143Ala
XM_006717005.4:c.427A>G	XP_006717068.1:p.Thr143Ala
NM_000507.4:c.673A>G MANE Select	NP_000498.2:p.Thr225Ala
NM_001127628.2:c.673A>G	NP_001121100.1:p.Thr225Ala