Canonical Allele Identifier: CA6418916
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6869299C>T , CM000674.2:g.6869299C>T GRCh38
NC_000012.11:g.6978463C>T , CM000674.1:g.6978463C>T GRCh37
NC_000012.10:g.6848724C>T NCBI36
NG_011948.1:g.6880C>T
NG_013308.1:g.9059G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.366C>T MANE Select ENSP00000379933.4:p.Leu122=
ENST00000229270.8:c.477C>T ENSP00000229270.4:p.Leu159=
ENST00000396705.9:c.366C>T ENSP00000379933.4:p.Leu122=
ENST00000488464.6:c.120C>T ENSP00000475620.1:p.Leu40=
ENST00000493987.5:c.120C>T ENSP00000475364.1:p.Leu40=
ENST00000495834.1:c.120C>T ENSP00000475829.1:p.Leu40=
ENST00000535434.5:c.120C>T ENSP00000443599.1:p.Leu40=
ENST00000613953.4:c.477C>T ENSP00000484435.1:p.Leu159=
NM_000365.5:c.366C>T NP_000356.1:p.Leu122=
NM_001159287.1:c.477C>T NP_001152759.1:p.Leu159=
NM_001258026.1:c.120C>T NP_001244955.1:p.Leu40=
XR_002957378.1:n.1099C>T
NM_000365.6:c.366C>T MANE Select NP_000356.1:p.Leu122=
NM_001258026.2:c.120C>T NP_001244955.1:p.Leu40=