Canonical Allele Identifier: CA2014289369
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6869785_6869788delinsCAGG , CM000674.2:g.6869785_6869788delinsCAGG GRCh38
NC_000012.11:g.6978949_6978952delinsCAGG , CM000674.1:g.6978949_6978952delinsCAGG GRCh37
NC_000012.10:g.6849210_6849213delinsCAGG NCBI36
NG_011948.1:g.7366_7369delinsCAGG
NG_013308.1:g.8570_8573delinsCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.543+12_543+15delinsCAGG MANE Select ENSP00000379933.4:n.543+12_543+15delinsCAGG
ENST00000229270.8:c.654+12_654+15delinsCAGG ENSP00000229270.4:n.654+12_654+15delinsCAGG
ENST00000396705.9:c.543+12_543+15delinsCAGG ENSP00000379933.4:n.543+12_543+15delinsCAGG
ENST00000482209.1:n.226+12_226+15delinsCAGG
ENST00000488464.6:c.297+12_297+15delinsCAGG ENSP00000475620.1:n.297+12_297+15delinsCAGG
ENST00000493987.5:c.297+12_297+15delinsCAGG ENSP00000475364.1:n.297+12_297+15delinsCAGG
ENST00000535434.5:c.297+12_297+15delinsCAGG ENSP00000443599.1:n.297+12_297+15delinsCAGG
ENST00000613953.4:c.654+12_654+15delinsCAGG ENSP00000484435.1:n.654+12_654+15delinsCAGG
NM_000365.5:c.543+12_543+15delinsCAGG NP_000356.1:n.543+12_543+15delinsCAGG
NM_001159287.1:c.654+12_654+15delinsCAGG NP_001152759.1:n.654+12_654+15delinsCAGG
NM_001258026.1:c.297+12_297+15delinsCAGG NP_001244955.1:n.297+12_297+15delinsCAGG
XR_002957378.1:n.1288_1291delinsCAGG
NM_000365.6:c.543+12_543+15delinsCAGG MANE Select NP_000356.1:n.543+12_543+15delinsCAGG
NM_001258026.2:c.297+12_297+15delinsCAGG NP_001244955.1:n.297+12_297+15delinsCAGG