Canonical Allele Identifier: CA2014289837
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870670_6870671delinsAG , CM000674.2:g.6870670_6870671delinsAG GRCh38
NC_000012.11:g.6979834_6979835delinsAG , CM000674.1:g.6979834_6979835delinsAG GRCh37
NC_000012.10:g.6850095_6850096delinsAG NCBI36
NG_011948.1:g.8251_8252delinsAG
NG_013308.1:g.7687_7688delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*287_*288delinsAG MANE Select ENSP00000379933.4:n.*287_*288delinsAG
ENST00000229270.8:c.*287_*288delinsAG ENSP00000229270.4:n.*287_*288delinsAG
ENST00000396705.9:c.*287_*288delinsAG ENSP00000379933.4:n.*287_*288delinsAG
ENST00000535434.5:c.*287_*288delinsAG ENSP00000443599.1:n.*287_*288delinsAG
ENST00000613953.4:c.*287_*288delinsAG ENSP00000484435.1:n.*287_*288delinsAG
NM_000365.5:c.*287_*288delinsAG NP_000356.1:n.*287_*288delinsAG
NM_001159287.1:c.*287_*288delinsAG NP_001152759.1:n.*287_*288delinsAG
NM_001258026.1:c.*287_*288delinsAG NP_001244955.1:n.*287_*288delinsAG
XR_002957378.1:n.2045_2046delinsAG
NM_000365.6:c.*287_*288delinsAG MANE Select NP_000356.1:n.*287_*288delinsAG
NM_001258026.2:c.*287_*288delinsAG NP_001244955.1:n.*287_*288delinsAG