Canonical Allele Identifier: CA383713880
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870324C>T , CM000674.2:g.6870324C>T GRCh38
NC_000012.11:g.6979488C>T , CM000674.1:g.6979488C>T GRCh37
NC_000012.10:g.6849749C>T NCBI36
NG_011948.1:g.7905C>T
NG_013308.1:g.8034G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.691C>T MANE Select ENSP00000379933.4:p.Leu231Phe
ENST00000229270.8:c.802C>T ENSP00000229270.4:p.Leu268Phe
ENST00000396705.9:c.691C>T ENSP00000379933.4:p.Leu231Phe
ENST00000474253.1:n.180C>T
ENST00000488464.6:c.445C>T ENSP00000475620.1:p.Leu149Phe
ENST00000535434.5:c.445C>T ENSP00000443599.1:p.Leu149Phe
ENST00000613953.4:c.802C>T ENSP00000484435.1:p.Leu268Phe
NM_000365.5:c.691C>T NP_000356.1:p.Leu231Phe
NM_001159287.1:c.802C>T NP_001152759.1:p.Leu268Phe
NM_001258026.1:c.445C>T NP_001244955.1:p.Leu149Phe
XR_002957378.1:n.1699C>T
NM_000365.6:c.691C>T MANE Select NP_000356.1:p.Leu231Phe
NM_001258026.2:c.445C>T NP_001244955.1:p.Leu149Phe