Canonical Allele Identifier: CA2617354470
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870023_6870024insA , CM000674.2:g.6870023_6870024insA GRCh38
NC_000012.11:g.6979187_6979188insA , CM000674.1:g.6979187_6979188insA GRCh37
NC_000012.10:g.6849448_6849449insA NCBI36
NG_011948.1:g.7604_7605insA
NG_013308.1:g.8334_8335insT

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.544-26_544-25insA MANE Select ENSP00000379933.4:n.544-26_544-25insA
ENST00000229270.8:c.655-26_655-25insA ENSP00000229270.4:n.655-26_655-25insA
ENST00000396705.9:c.544-26_544-25insA ENSP00000379933.4:n.544-26_544-25insA
ENST00000474253.1:n.7_8insA
ENST00000482209.1:n.227-13_227-12insA
ENST00000488464.6:c.298-26_298-25insA ENSP00000475620.1:n.298-26_298-25insA
ENST00000493987.5:c.298-26_298-25insA ENSP00000475364.1:n.298-26_298-25insA
ENST00000535434.5:c.298-26_298-25insA ENSP00000443599.1:n.298-26_298-25insA
ENST00000613953.4:c.655-26_655-25insA ENSP00000484435.1:n.655-26_655-25insA
NM_000365.5:c.544-26_544-25insA NP_000356.1:n.544-26_544-25insA
NM_001159287.1:c.655-26_655-25insA NP_001152759.1:n.655-26_655-25insA
NM_001258026.1:c.298-26_298-25insA NP_001244955.1:n.298-26_298-25insA
XR_002957378.1:n.1526_1527insA
NM_000365.6:c.544-26_544-25insA MANE Select NP_000356.1:n.544-26_544-25insA
NM_001258026.2:c.298-26_298-25insA NP_001244955.1:n.298-26_298-25insA