Canonical Allele Identifier: CA2014288930
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6868868_6868876delinsGGTTTGTGC , CM000674.2:g.6868868_6868876delinsGGTTTGTGC GRCh38
NC_000012.11:g.6978032_6978040delinsGGTTTGTGC , CM000674.1:g.6978032_6978040delinsGGTTTGTGC GRCh37
NC_000012.10:g.6848293_6848301delinsGGTTTGTGC NCBI36
NG_011948.1:g.6449_6457delinsGGTTTGTGC

Transcript Alleles

HGVS Amino-acid change
ENST00000396705.10:c.120_128delinsGGTTTGTGC MANE Select ENSP00000379933.4:p.Val40=
ENST00000229270.8:c.231_239delinsGGTTTGTGC ENSP00000229270.4:p.Val77=
ENST00000396705.9:c.120_128delinsGGTTTGTGC ENSP00000379933.4:p.Val40=
ENST00000462761.5:c.-127_-119delinsGGTTTGTGC ENSP00000475184.1:n.-127_-119delinsGGTTTG...
ENST00000488464.6:c.-127_-119delinsGGTTTGTGC ENSP00000475620.1:n.-127_-119delinsGGTTTG...
ENST00000493987.5:c.-127_-119delinsGGTTTGTGC ENSP00000475364.1:n.-127_-119delinsGGTTTG...
ENST00000495834.1:c.-127_-119delinsGGTTTGTGC ENSP00000475829.1:n.-127_-119delinsGGTTTG...
ENST00000535434.5:c.-127_-119delinsGGTTTGTGC ENSP00000443599.1:n.-127_-119delinsGGTTTG...
ENST00000613953.4:c.231_239delinsGGTTTGTGC ENSP00000484435.1:p.Val77=
NM_000365.5:c.120_128delinsGGTTTGTGC NP_000356.1:p.Val40=
NM_001159287.1:c.231_239delinsGGTTTGTGC NP_001152759.1:p.Val77=
NM_001258026.1:c.-127_-119delinsGGTTTGTGC NP_001244955.1:n.-127_-119delinsGGTTTGTGC...
XR_002957378.1:n.853_861delinsGGTTTGTGC
NM_000365.6:c.120_128delinsGGTTTGTGC MANE Select NP_000356.1:p.Val40=
NM_001258026.2:c.-127_-119delinsGGTTTGTGC NP_001244955.1:n.-127_-119delinsGGTTTGTGC...