Canonical Allele Identifier: CA2014289476
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870002_6870003delinsCT , CM000674.2:g.6870002_6870003delinsCT GRCh38
NC_000012.11:g.6979166_6979167delinsCT , CM000674.1:g.6979166_6979167delinsCT GRCh37
NC_000012.10:g.6849427_6849428delinsCT NCBI36
NG_011948.1:g.7583_7584delinsCT
NG_013308.1:g.8355_8356delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.544-47_544-46delinsCT MANE Select ENSP00000379933.4:n.544-47_544-46delinsCT
ENST00000229270.8:c.655-47_655-46delinsCT ENSP00000229270.4:n.655-47_655-46delinsCT
ENST00000396705.9:c.544-47_544-46delinsCT ENSP00000379933.4:n.544-47_544-46delinsCT
ENST00000482209.1:n.227-34_227-33delinsCT
ENST00000488464.6:c.298-47_298-46delinsCT ENSP00000475620.1:n.298-47_298-46delinsCT
ENST00000493987.5:c.298-47_298-46delinsCT ENSP00000475364.1:n.298-47_298-46delinsCT
ENST00000535434.5:c.298-47_298-46delinsCT ENSP00000443599.1:n.298-47_298-46delinsCT
ENST00000613953.4:c.655-47_655-46delinsCT ENSP00000484435.1:n.655-47_655-46delinsCT
NM_000365.5:c.544-47_544-46delinsCT NP_000356.1:n.544-47_544-46delinsCT
NM_001159287.1:c.655-47_655-46delinsCT NP_001152759.1:n.655-47_655-46delinsCT
NM_001258026.1:c.298-47_298-46delinsCT NP_001244955.1:n.298-47_298-46delinsCT
XR_002957378.1:n.1505_1506delinsCT
NM_000365.6:c.544-47_544-46delinsCT MANE Select NP_000356.1:n.544-47_544-46delinsCT
NM_001258026.2:c.298-47_298-46delinsCT NP_001244955.1:n.298-47_298-46delinsCT