Canonical Allele Identifier: CA2014289844
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870677_6870678delinsAG , CM000674.2:g.6870677_6870678delinsAG GRCh38
NC_000012.11:g.6979841_6979842delinsAG , CM000674.1:g.6979841_6979842delinsAG GRCh37
NC_000012.10:g.6850102_6850103delinsAG NCBI36
NG_011948.1:g.8258_8259delinsAG
NG_013308.1:g.7680_7681delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*294_*295delinsAG MANE Select ENSP00000379933.4:n.*294_*295delinsAG
ENST00000229270.8:c.*294_*295delinsAG ENSP00000229270.4:n.*294_*295delinsAG
ENST00000396705.9:c.*294_*295delinsAG ENSP00000379933.4:n.*294_*295delinsAG
ENST00000535434.5:c.*294_*295delinsAG ENSP00000443599.1:n.*294_*295delinsAG
ENST00000613953.4:c.*294_*295delinsAG ENSP00000484435.1:n.*294_*295delinsAG
NM_000365.5:c.*294_*295delinsAG NP_000356.1:n.*294_*295delinsAG
NM_001159287.1:c.*294_*295delinsAG NP_001152759.1:n.*294_*295delinsAG
NM_001258026.1:c.*294_*295delinsAG NP_001244955.1:n.*294_*295delinsAG
XR_002957378.1:n.2052_2053delinsAG
NM_000365.6:c.*294_*295delinsAG MANE Select NP_000356.1:n.*294_*295delinsAG
NM_001258026.2:c.*294_*295delinsAG NP_001244955.1:n.*294_*295delinsAG