Canonical Allele Identifier: CA2564307841
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870556_6870594del , CM000674.2:g.6870556_6870594del GRCh38
NC_000012.11:g.6979720_6979758del , CM000674.1:g.6979720_6979758del GRCh37
NC_000012.10:g.6849981_6850019del NCBI36
NG_011948.1:g.8137_8175del
NG_013308.1:g.7774_7812del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*173_*211del MANE Select ENSP00000379933.4:n.*173_*211del
ENST00000229270.8:c.*173_*211del ENSP00000229270.4:n.*173_*211del
ENST00000396705.9:c.*173_*211del ENSP00000379933.4:n.*173_*211del
ENST00000535434.5:c.*173_*211del ENSP00000443599.1:n.*173_*211del
ENST00000613953.4:c.*173_*211del ENSP00000484435.1:n.*173_*211del
NM_000365.5:c.*173_*211del NP_000356.1:n.*173_*211del
NM_001159287.1:c.*173_*211del NP_001152759.1:n.*173_*211del
NM_001258026.1:c.*173_*211del NP_001244955.1:n.*173_*211del
XR_002957378.1:n.1931_1969del
NM_000365.6:c.*173_*211del MANE Select NP_000356.1:n.*173_*211del
NM_001258026.2:c.*173_*211del NP_001244955.1:n.*173_*211del