Canonical Allele Identifier: CA2014288937
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6868880C= , CM000674.2:g.6868880C= GRCh38
NC_000012.11:g.6978044C= , CM000674.1:g.6978044C= GRCh37
NC_000012.10:g.6848305C= NCBI36
NG_011948.1:g.6461C=

Transcript Alleles

HGVS Amino-acid change
ENST00000396705.10:c.132C= MANE Select ENSP00000379933.4:p.Pro44=
ENST00000229270.8:c.243C= ENSP00000229270.4:p.Pro81=
ENST00000396705.9:c.132C= ENSP00000379933.4:p.Pro44=
ENST00000462761.5:c.-115C= ENSP00000475184.1:n.-115C=
ENST00000488464.6:c.-115C= ENSP00000475620.1:n.-115C=
ENST00000493987.5:c.-115C= ENSP00000475364.1:n.-115C=
ENST00000495834.1:c.-115C= ENSP00000475829.1:n.-115C=
ENST00000535434.5:c.-115C= ENSP00000443599.1:n.-115C=
ENST00000613953.4:c.243C= ENSP00000484435.1:p.Pro81=
NM_000365.5:c.132C= NP_000356.1:p.Pro44=
NM_001159287.1:c.243C= NP_001152759.1:p.Pro81=
NM_001258026.1:c.-115C= NP_001244955.1:n.-115C=
XR_002957378.1:n.865C=
NM_000365.6:c.132C= MANE Select NP_000356.1:p.Pro44=
NM_001258026.2:c.-115C= NP_001244955.1:n.-115C=