Canonical Allele Identifier: CA383713811
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870315G>T , CM000674.2:g.6870315G>T GRCh38
NC_000012.11:g.6979479G>T , CM000674.1:g.6979479G>T GRCh37
NC_000012.10:g.6849740G>T NCBI36
NG_011948.1:g.7896G>T
NG_013308.1:g.8043C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.682G>T MANE Select ENSP00000379933.4:p.Asp228Tyr
ENST00000229270.8:c.793G>T ENSP00000229270.4:p.Asp265Tyr
ENST00000396705.9:c.682G>T ENSP00000379933.4:p.Asp228Tyr
ENST00000474253.1:n.171G>T
ENST00000488464.6:c.436G>T ENSP00000475620.1:p.Asp146Tyr
ENST00000535434.5:c.436G>T ENSP00000443599.1:p.Asp146Tyr
ENST00000613953.4:c.793G>T ENSP00000484435.1:p.Asp265Tyr
NM_000365.5:c.682G>T NP_000356.1:p.Asp228Tyr
NM_001159287.1:c.793G>T NP_001152759.1:p.Asp265Tyr
NM_001258026.1:c.436G>T NP_001244955.1:p.Asp146Tyr
XR_002957378.1:n.1690G>T
NM_000365.6:c.682G>T MANE Select NP_000356.1:p.Asp228Tyr
NM_001258026.2:c.436G>T NP_001244955.1:p.Asp146Tyr