Canonical Allele Identifier: CA2014289672
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870384_6870385delinsGC , CM000674.2:g.6870384_6870385delinsGC GRCh38
NC_000012.11:g.6979548_6979549delinsGC , CM000674.1:g.6979548_6979549delinsGC GRCh37
NC_000012.10:g.6849809_6849810delinsGC NCBI36
NG_011948.1:g.7965_7966delinsGC
NG_013308.1:g.7973_7974delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*1_*2delinsGC MANE Select ENSP00000379933.4:n.*1_*2delinsGC
ENST00000229270.8:c.*1_*2delinsGC ENSP00000229270.4:n.*1_*2delinsGC
ENST00000396705.9:c.*1_*2delinsGC ENSP00000379933.4:n.*1_*2delinsGC
ENST00000474253.1:n.240_241delinsGC
ENST00000535434.5:c.*1_*2delinsGC ENSP00000443599.1:n.*1_*2delinsGC
ENST00000613953.4:c.*1_*2delinsGC ENSP00000484435.1:n.*1_*2delinsGC
NM_000365.5:c.*1_*2delinsGC NP_000356.1:n.*1_*2delinsGC
NM_001159287.1:c.*1_*2delinsGC NP_001152759.1:n.*1_*2delinsGC
NM_001258026.1:c.*1_*2delinsGC NP_001244955.1:n.*1_*2delinsGC
XR_002957378.1:n.1759_1760delinsGC
NM_000365.6:c.*1_*2delinsGC MANE Select NP_000356.1:n.*1_*2delinsGC
NM_001258026.2:c.*1_*2delinsGC NP_001244955.1:n.*1_*2delinsGC