Canonical Allele Identifier: CA2014289518
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870070C= , CM000674.2:g.6870070C= GRCh38
NC_000012.11:g.6979234C= , CM000674.1:g.6979234C= GRCh37
NC_000012.10:g.6849495C= NCBI36
NG_011948.1:g.7651C=
NG_013308.1:g.8288G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.565C= MANE Select ENSP00000379933.4:p.Leu189=
ENST00000229270.8:c.676C= ENSP00000229270.4:p.Leu226=
ENST00000396705.9:c.565C= ENSP00000379933.4:p.Leu189=
ENST00000474253.1:n.54C=
ENST00000482209.1:n.261C=
ENST00000488464.6:c.319C= ENSP00000475620.1:p.Leu107=
ENST00000493987.5:c.319C= ENSP00000475364.1:p.Leu107=
ENST00000535434.5:c.319C= ENSP00000443599.1:p.Leu107=
ENST00000613953.4:c.676C= ENSP00000484435.1:p.Leu226=
NM_000365.5:c.565C= NP_000356.1:p.Leu189=
NM_001159287.1:c.676C= NP_001152759.1:p.Leu226=
NM_001258026.1:c.319C= NP_001244955.1:p.Leu107=
XR_002957378.1:n.1573C=
NM_000365.6:c.565C= MANE Select NP_000356.1:p.Leu189=
NM_001258026.2:c.319C= NP_001244955.1:p.Leu107=