Canonical Allele Identifier: CA2794431093
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870637del , CM000674.2:g.6870637del GRCh38
NC_000012.11:g.6979801del , CM000674.1:g.6979801del GRCh37
NC_000012.10:g.6850062del NCBI36
NG_011948.1:g.8218del
NG_013308.1:g.7722del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*254del MANE Select ENSP00000379933.4:n.*254del
ENST00000229270.8:c.*254del ENSP00000229270.4:n.*254del
ENST00000396705.9:c.*254del ENSP00000379933.4:n.*254del
ENST00000535434.5:c.*254del ENSP00000443599.1:n.*254del
ENST00000613953.4:c.*254del ENSP00000484435.1:n.*254del
NM_000365.5:c.*254del NP_000356.1:n.*254del
NM_001159287.1:c.*254del NP_001152759.1:n.*254del
NM_001258026.1:c.*254del NP_001244955.1:n.*254del
XR_002957378.1:n.2012del
NM_000365.6:c.*254del MANE Select NP_000356.1:n.*254del
NM_001258026.2:c.*254del NP_001244955.1:n.*254del