Canonical Allele Identifier: CA383712856
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870076G>C , CM000674.2:g.6870076G>C GRCh38
NC_000012.11:g.6979240G>C , CM000674.1:g.6979240G>C GRCh37
NC_000012.10:g.6849501G>C NCBI36
NG_011948.1:g.7657G>C
NG_013308.1:g.8282C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.571G>C MANE Select ENSP00000379933.4:p.Gly191Arg
ENST00000229270.8:c.682G>C ENSP00000229270.4:p.Gly228Arg
ENST00000396705.9:c.571G>C ENSP00000379933.4:p.Gly191Arg
ENST00000474253.1:n.60G>C
ENST00000482209.1:n.267G>C
ENST00000488464.6:c.325G>C ENSP00000475620.1:p.Gly109Arg
ENST00000493987.5:c.325G>C ENSP00000475364.1:p.Gly109Arg
ENST00000535434.5:c.325G>C ENSP00000443599.1:p.Gly109Arg
ENST00000613953.4:c.682G>C ENSP00000484435.1:p.Gly228Arg
NM_000365.5:c.571G>C NP_000356.1:p.Gly191Arg
NM_001159287.1:c.682G>C NP_001152759.1:p.Gly228Arg
NM_001258026.1:c.325G>C NP_001244955.1:p.Gly109Arg
XR_002957378.1:n.1579G>C
NM_000365.6:c.571G>C MANE Select NP_000356.1:p.Gly191Arg
NM_001258026.2:c.325G>C NP_001244955.1:p.Gly109Arg