Canonical Allele Identifier: CA2794431095
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870672_6870678del , CM000674.2:g.6870672_6870678del GRCh38
NC_000012.11:g.6979836_6979842del , CM000674.1:g.6979836_6979842del GRCh37
NC_000012.10:g.6850097_6850103del NCBI36
NG_011948.1:g.8253_8259del
NG_013308.1:g.7686_7692del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.*289_*295del MANE Select ENSP00000379933.4:n.*289_*295del
ENST00000229270.8:c.*289_*295del ENSP00000229270.4:n.*289_*295del
ENST00000396705.9:c.*289_*295del ENSP00000379933.4:n.*289_*295del
ENST00000535434.5:c.*289_*295del ENSP00000443599.1:n.*289_*295del
ENST00000613953.4:c.*289_*295del ENSP00000484435.1:n.*289_*295del
NM_000365.5:c.*289_*295del NP_000356.1:n.*289_*295del
NM_001159287.1:c.*289_*295del NP_001152759.1:n.*289_*295del
NM_001258026.1:c.*289_*295del NP_001244955.1:n.*289_*295del
XR_002957378.1:n.2047_2053del
NM_000365.6:c.*289_*295del MANE Select NP_000356.1:n.*289_*295del
NM_001258026.2:c.*289_*295del NP_001244955.1:n.*289_*295del