Canonical Allele Identifier: CA2575062115
Gene: TPI1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6869805del , CM000674.2:g.6869805del GRCh38
NC_000012.11:g.6978969del , CM000674.1:g.6978969del GRCh37
NC_000012.10:g.6849230del NCBI36
NG_011948.1:g.7386del
NG_013308.1:g.8555del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.543+32del MANE Select ENSP00000379933.4:n.543+32del
ENST00000229270.8:c.654+32del ENSP00000229270.4:n.654+32del
ENST00000396705.9:c.543+32del ENSP00000379933.4:n.543+32del
ENST00000482209.1:n.226+32del
ENST00000488464.6:c.297+32del ENSP00000475620.1:n.297+32del
ENST00000493987.5:c.297+32del ENSP00000475364.1:n.297+32del
ENST00000535434.5:c.297+32del ENSP00000443599.1:n.297+32del
ENST00000613953.4:c.654+32del ENSP00000484435.1:n.654+32del
NM_000365.5:c.543+32del NP_000356.1:n.543+32del
NM_001159287.1:c.654+32del NP_001152759.1:n.654+32del
NM_001258026.1:c.297+32del NP_001244955.1:n.297+32del
XR_002957378.1:n.1308del
NM_000365.6:c.543+32del MANE Select NP_000356.1:n.543+32del
NM_001258026.2:c.297+32del NP_001244955.1:n.297+32del