Canonical Allele Identifier: CA1865264733

Gene: FBP1

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.94638836_94638837delinsGA , CM000671.2:g.94638836_94638837delinsGA	GRCh38
NC_000009.11:g.97401118_97401119delinsGA , CM000671.1:g.97401118_97401119delinsGA	GRCh37
NC_000009.10:g.96440939_96440940delinsGA	NCBI36
NG_008174.1:g.6413_6414delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682520.1:c.170+304_170+305delinsTC	ENSP00000507547.1:n.170+304_170+305delinsTC
ENST00000375326.9:c.170+304_170+305delinsTC MANE Select	ENSP00000364475.5:n.170+304_170+305delinsTC
ENST00000375326.8:c.170+304_170+305delinsTC	ENSP00000364475.4:n.170+304_170+305delinsTC
ENST00000414122.1:c.-83+1207_-83+1208delinsTC	ENSP00000411619.1:n.-83+1207_-83+1208delinsTC
ENST00000415431.5:c.170+304_170+305delinsTC	ENSP00000408025.1:n.170+304_170+305delinsTC
NM_000507.3:c.170+304_170+305delinsTC	NP_000498.2:n.170+304_170+305delinsTC
NM_001127628.1:c.170+304_170+305delinsTC	NP_001121100.1:n.170+304_170+305delinsTC
XM_006717005.2:c.-77+1207_-77+1208delinsTC	XP_006717068.1:n.-77+1207_-77+1208delinsTC
XM_006717005.4:c.-77+1207_-77+1208delinsTC	XP_006717068.1:n.-77+1207_-77+1208delinsTC
NM_000507.4:c.170+304_170+305delinsTC MANE Select	NP_000498.2:n.170+304_170+305delinsTC
NM_001127628.2:c.170+304_170+305delinsTC	NP_001121100.1:n.170+304_170+305delinsTC