Canonical Allele Identifier: CA2575062145
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870210del , CM000674.2:g.6870210del GRCh38
NC_000012.11:g.6979374del , CM000674.1:g.6979374del GRCh37
NC_000012.10:g.6849635del NCBI36
NG_011948.1:g.7791del
NG_013308.1:g.8151del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.632-55del MANE Select ENSP00000379933.4:n.632-55del
ENST00000229270.8:c.743-55del ENSP00000229270.4:n.743-55del
ENST00000396705.9:c.632-55del ENSP00000379933.4:n.632-55del
ENST00000474253.1:n.121-55del
ENST00000488464.6:c.386-55del ENSP00000475620.1:n.386-55del
ENST00000535434.5:c.386-55del ENSP00000443599.1:n.386-55del
ENST00000613953.4:c.743-55del ENSP00000484435.1:n.743-55del
NM_000365.5:c.632-55del NP_000356.1:n.632-55del
NM_001159287.1:c.743-55del NP_001152759.1:n.743-55del
NM_001258026.1:c.386-55del NP_001244955.1:n.386-55del
XR_002957378.1:n.1640-55del
NM_000365.6:c.632-55del MANE Select NP_000356.1:n.632-55del
NM_001258026.2:c.386-55del NP_001244955.1:n.386-55del