Canonical Allele Identifier: CA2794431068
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870217del , CM000674.2:g.6870217del GRCh38
NC_000012.11:g.6979381del , CM000674.1:g.6979381del GRCh37
NC_000012.10:g.6849642del NCBI36
NG_011948.1:g.7798del
NG_013308.1:g.8141del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.632-48del MANE Select ENSP00000379933.4:n.632-48del
ENST00000229270.8:c.743-48del ENSP00000229270.4:n.743-48del
ENST00000396705.9:c.632-48del ENSP00000379933.4:n.632-48del
ENST00000474253.1:n.121-48del
ENST00000488464.6:c.386-48del ENSP00000475620.1:n.386-48del
ENST00000535434.5:c.386-48del ENSP00000443599.1:n.386-48del
ENST00000613953.4:c.743-48del ENSP00000484435.1:n.743-48del
NM_000365.5:c.632-48del NP_000356.1:n.632-48del
NM_001159287.1:c.743-48del NP_001152759.1:n.743-48del
NM_001258026.1:c.386-48del NP_001244955.1:n.386-48del
XR_002957378.1:n.1640-48del
NM_000365.6:c.632-48del MANE Select NP_000356.1:n.632-48del
NM_001258026.2:c.386-48del NP_001244955.1:n.386-48del