Canonical Allele Identifier: CA2014289447
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6869944G= , CM000674.2:g.6869944G= GRCh38
NC_000012.11:g.6979108G= , CM000674.1:g.6979108G= GRCh37
NC_000012.10:g.6849369G= NCBI36
NG_011948.1:g.7525G=
NG_013308.1:g.8414C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.544-105G= MANE Select ENSP00000379933.4:n.544-105G=
ENST00000229270.8:c.655-105G= ENSP00000229270.4:n.655-105G=
ENST00000396705.9:c.544-105G= ENSP00000379933.4:n.544-105G=
ENST00000482209.1:n.227-92G=
ENST00000488464.6:c.298-105G= ENSP00000475620.1:n.298-105G=
ENST00000493987.5:c.298-105G= ENSP00000475364.1:n.298-105G=
ENST00000535434.5:c.298-105G= ENSP00000443599.1:n.298-105G=
ENST00000613953.4:c.655-105G= ENSP00000484435.1:n.655-105G=
NM_000365.5:c.544-105G= NP_000356.1:n.544-105G=
NM_001159287.1:c.655-105G= NP_001152759.1:n.655-105G=
NM_001258026.1:c.298-105G= NP_001244955.1:n.298-105G=
XR_002957378.1:n.1447G=
NM_000365.6:c.544-105G= MANE Select NP_000356.1:n.544-105G=
NM_001258026.2:c.298-105G= NP_001244955.1:n.298-105G=