Canonical Allele Identifier: CA2617354417
Gene: TPI1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6870009_6870010del , CM000674.2:g.6870009_6870010del GRCh38
NC_000012.11:g.6979173_6979174del , CM000674.1:g.6979173_6979174del GRCh37
NC_000012.10:g.6849434_6849435del NCBI36
NG_011948.1:g.7590_7591del
NG_013308.1:g.8352_8353del

Transcript Alleles

HGVS Amino-acid Change
ENST00000396705.10:c.544-40_544-39del MANE Select ENSP00000379933.4:n.544-40_544-39del
ENST00000229270.8:c.655-40_655-39del ENSP00000229270.4:n.655-40_655-39del
ENST00000396705.9:c.544-40_544-39del ENSP00000379933.4:n.544-40_544-39del
ENST00000482209.1:n.227-27_227-26del
ENST00000488464.6:c.298-40_298-39del ENSP00000475620.1:n.298-40_298-39del
ENST00000493987.5:c.298-40_298-39del ENSP00000475364.1:n.298-40_298-39del
ENST00000535434.5:c.298-40_298-39del ENSP00000443599.1:n.298-40_298-39del
ENST00000613953.4:c.655-40_655-39del ENSP00000484435.1:n.655-40_655-39del
NM_000365.5:c.544-40_544-39del NP_000356.1:n.544-40_544-39del
NM_001159287.1:c.655-40_655-39del NP_001152759.1:n.655-40_655-39del
NM_001258026.1:c.298-40_298-39del NP_001244955.1:n.298-40_298-39del
XR_002957378.1:n.1512_1513del
NM_000365.6:c.544-40_544-39del MANE Select NP_000356.1:n.544-40_544-39del
NM_001258026.2:c.298-40_298-39del NP_001244955.1:n.298-40_298-39del