Canonical Allele Identifier: CA1844867864
Gene: APTX HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33014400_33014401delinsGA , CM000671.2:g.33014400_33014401delinsGA GRCh38
NC_000009.11:g.33014398_33014399delinsGA , CM000671.1:g.33014398_33014399delinsGA GRCh37
NC_000009.10:g.33004398_33004399delinsGA NCBI36
NG_012821.2:g.15731_15732delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000436040.7:c.-5+10622_-5+10623delinsTC ENSP00000400806.4:n.-5+10622_-5+10623delinsTC
ENST00000460940.6:c.-5+10599_-5+10600delinsTC ENSP00000418311.1:n.-5+10599_-5+10600delinsTC
ENST00000467331.6:c.-5+10403_-5+10404delinsTC ENSP00000418733.1:n.-5+10403_-5+10404delinsTC
ENST00000468275.6:c.-5+10403_-5+10404delinsTC ENSP00000420263.2:n.-5+10403_-5+10404delinsTC
ENST00000482687.6:c.-5+10403_-5+10404delinsTC ENSP00000419289.2:n.-5+10403_-5+10404delinsTC
ENST00000485479.6:c.-5+10599_-5+10600delinsTC ENSP00000418144.1:n.-5+10599_-5+10600delinsTC
ENST00000495360.6:c.-5+10599_-5+10600delinsTC ENSP00000419623.2:n.-5+10599_-5+10600delinsTC
ENST00000672281.1:n.193+3275_193+3276delinsTC
ENST00000673248.1:c.-127+10403_-127+10404delinsTC ENSP00000500601.1:n.-127+10403_-127+10404delinsTC
ENST00000673360.1:c.-5+10403_-5+10404delinsTC ENSP00000500360.1:n.-5+10403_-5+10404delinsTC
ENST00000673487.1:c.-5+10403_-5+10404delinsTC ENSP00000500943.1:n.-5+10403_-5+10404delinsTC
ENST00000460945.5:n.169+10599_169+10600delinsTC
ENST00000495360.5:c.-5+10403_-5+10404delinsTC ENSP00000419623.1:n.-5+10403_-5+10404delinsTC
XM_011517936.1:c.-264+10622_-264+10623delinsTC XP_011516238.1:n.-264+10622_-264+10623delinsTC
XM_011517937.1:c.-222+10599_-222+10600delinsTC XP_011516239.1:n.-222+10599_-222+10600delinsTC
XM_017014837.2:c.-5+10403_-5+10404delinsTC XP_016870326.1:n.-5+10403_-5+10404delinsTC
XM_024447575.1:c.-5+10403_-5+10404delinsTC XP_024303343.1:n.-5+10403_-5+10404delinsTC
XM_024447576.1:c.-5+10599_-5+10600delinsTC XP_024303344.1:n.-5+10599_-5+10600delinsTC
XM_024447577.1:c.-5+10622_-5+10623delinsTC XP_024303345.1:n.-5+10622_-5+10623delinsTC
XM_024447579.1:c.-5+10403_-5+10404delinsTC XP_024303347.1:n.-5+10403_-5+10404delinsTC
XM_024447580.1:c.-5+10622_-5+10623delinsTC XP_024303348.1:n.-5+10622_-5+10623delinsTC
XM_024447581.1:c.-264+10403_-264+10404delinsTC XP_024303349.1:n.-264+10403_-264+10404delinsTC
XM_024447582.1:c.-264+10599_-264+10600delinsTC XP_024303350.1:n.-264+10599_-264+10600delinsTC
NM_001368995.1:c.-5+10599_-5+10600delinsTC NP_001355924.1:n.-5+10599_-5+10600delinsTC
NM_001368996.1:c.-5+10622_-5+10623delinsTC NP_001355925.1:n.-5+10622_-5+10623delinsTC
NM_001368997.1:c.-5+10403_-5+10404delinsTC NP_001355926.1:n.-5+10403_-5+10404delinsTC
NM_001368999.1:c.-5+10403_-5+10404delinsTC NP_001355928.1:n.-5+10403_-5+10404delinsTC
NM_001369000.1:c.-5+10403_-5+10404delinsTC NP_001355929.1:n.-5+10403_-5+10404delinsTC
NM_001369001.1:c.-5+10622_-5+10623delinsTC NP_001355930.1:n.-5+10622_-5+10623delinsTC
NM_001369002.1:c.-264+10599_-264+10600delinsTC NP_001355931.1:n.-264+10599_-264+10600delinsTC
NM_001369003.1:c.-264+10403_-264+10404delinsTC NP_001355932.1:n.-264+10403_-264+10404delinsTC
NR_160922.1:n.317+10403_317+10404delinsTC
NR_160923.1:n.121+10599_121+10600delinsTC
NR_160924.1:n.121+10599_121+10600delinsTC
NR_160925.1:n.317+10403_317+10404delinsTC
NR_160926.1:n.121+10599_121+10600delinsTC
NR_160927.1:n.317+10403_317+10404delinsTC
NR_160928.1:n.317+10403_317+10404delinsTC
NR_160929.1:n.121+10599_121+10600delinsTC