Canonical Allele Identifier: CA1844868353
Gene: APTX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33014750_33014751delinsAG , CM000671.2:g.33014750_33014751delinsAG GRCh38
NC_000009.11:g.33014748_33014749delinsAG , CM000671.1:g.33014748_33014749delinsAG GRCh37
NC_000009.10:g.33004748_33004749delinsAG NCBI36
NG_012821.2:g.15381_15382delinsCT

Transcript Alleles

HGVS Amino-acid change
ENST00000436040.7:c.-5+10272_-5+10273delinsCT ENSP00000400806.4:n.-5+10272_-5+10273deli...
ENST00000460940.6:c.-5+10249_-5+10250delinsCT ENSP00000418311.1:n.-5+10249_-5+10250deli...
ENST00000467331.6:c.-5+10053_-5+10054delinsCT ENSP00000418733.1:n.-5+10053_-5+10054deli...
ENST00000468275.6:c.-5+10053_-5+10054delinsCT ENSP00000420263.2:n.-5+10053_-5+10054deli...
ENST00000482687.6:c.-5+10053_-5+10054delinsCT ENSP00000419289.2:n.-5+10053_-5+10054deli...
ENST00000485479.6:c.-5+10249_-5+10250delinsCT ENSP00000418144.1:n.-5+10249_-5+10250deli...
ENST00000495360.6:c.-5+10249_-5+10250delinsCT ENSP00000419623.2:n.-5+10249_-5+10250deli...
ENST00000672281.1:n.193+2925_193+2926delinsCT
ENST00000673248.1:c.-127+10053_-127+10054delinsCT ENSP00000500601.1:n.-127+10053_-127+10054...
ENST00000673360.1:c.-5+10053_-5+10054delinsCT ENSP00000500360.1:n.-5+10053_-5+10054deli...
ENST00000673487.1:c.-5+10053_-5+10054delinsCT ENSP00000500943.1:n.-5+10053_-5+10054deli...
ENST00000460945.5:n.169+10249_169+10250delinsCT
ENST00000495360.5:c.-5+10053_-5+10054delinsCT ENSP00000419623.1:n.-5+10053_-5+10054deli...
XM_011517936.1:c.-264+10272_-264+10273delinsCT XP_011516238.1:n.-264+10272_-264+10273del...
XM_011517937.1:c.-222+10249_-222+10250delinsCT XP_011516239.1:n.-222+10249_-222+10250del...
XM_017014837.2:c.-5+10053_-5+10054delinsCT XP_016870326.1:n.-5+10053_-5+10054delinsC...
XM_024447575.1:c.-5+10053_-5+10054delinsCT XP_024303343.1:n.-5+10053_-5+10054delinsC...
XM_024447576.1:c.-5+10249_-5+10250delinsCT XP_024303344.1:n.-5+10249_-5+10250delinsC...
XM_024447577.1:c.-5+10272_-5+10273delinsCT XP_024303345.1:n.-5+10272_-5+10273delinsC...
XM_024447579.1:c.-5+10053_-5+10054delinsCT XP_024303347.1:n.-5+10053_-5+10054delinsC...
XM_024447580.1:c.-5+10272_-5+10273delinsCT XP_024303348.1:n.-5+10272_-5+10273delinsC...
XM_024447581.1:c.-264+10053_-264+10054delinsCT XP_024303349.1:n.-264+10053_-264+10054del...
XM_024447582.1:c.-264+10249_-264+10250delinsCT XP_024303350.1:n.-264+10249_-264+10250del...
NM_001368995.1:c.-5+10249_-5+10250delinsCT NP_001355924.1:n.-5+10249_-5+10250delinsC...
NM_001368996.1:c.-5+10272_-5+10273delinsCT NP_001355925.1:n.-5+10272_-5+10273delinsC...
NM_001368997.1:c.-5+10053_-5+10054delinsCT NP_001355926.1:n.-5+10053_-5+10054delinsC...
NM_001368999.1:c.-5+10053_-5+10054delinsCT NP_001355928.1:n.-5+10053_-5+10054delinsC...
NM_001369000.1:c.-5+10053_-5+10054delinsCT NP_001355929.1:n.-5+10053_-5+10054delinsC...
NM_001369001.1:c.-5+10272_-5+10273delinsCT NP_001355930.1:n.-5+10272_-5+10273delinsC...
NM_001369002.1:c.-264+10249_-264+10250delinsCT NP_001355931.1:n.-264+10249_-264+10250del...
NM_001369003.1:c.-264+10053_-264+10054delinsCT NP_001355932.1:n.-264+10053_-264+10054del...
NR_160922.1:n.317+10053_317+10054delinsCT
NR_160923.1:n.121+10249_121+10250delinsCT
NR_160924.1:n.121+10249_121+10250delinsCT
NR_160925.1:n.317+10053_317+10054delinsCT
NR_160926.1:n.121+10249_121+10250delinsCT
NR_160927.1:n.317+10053_317+10054delinsCT
NR_160928.1:n.317+10053_317+10054delinsCT
NR_160929.1:n.121+10249_121+10250delinsCT