Canonical Allele Identifier: CA863342774
Gene: APTX HGNC NCBI

Linked Data

dbSNP Id: rs1279343939

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.33014721_33014722insA , CM000671.2:g.33014721_33014722insA GRCh38
NC_000009.11:g.33014719_33014720insA , CM000671.1:g.33014719_33014720insA GRCh37
NC_000009.10:g.33004719_33004720insA NCBI36
NG_012821.2:g.15410_15411insT

Transcript Alleles

HGVS Amino-acid change
ENST00000436040.7:c.-5+10301_-5+10302insT ENSP00000400806.4:n.-5+10301_-5+10302insT...
ENST00000460940.6:c.-5+10278_-5+10279insT ENSP00000418311.1:n.-5+10278_-5+10279insT...
ENST00000467331.6:c.-5+10082_-5+10083insT ENSP00000418733.1:n.-5+10082_-5+10083insT...
ENST00000468275.6:c.-5+10082_-5+10083insT ENSP00000420263.2:n.-5+10082_-5+10083insT...
ENST00000482687.6:c.-5+10082_-5+10083insT ENSP00000419289.2:n.-5+10082_-5+10083insT...
ENST00000485479.6:c.-5+10278_-5+10279insT ENSP00000418144.1:n.-5+10278_-5+10279insT...
ENST00000495360.6:c.-5+10278_-5+10279insT ENSP00000419623.2:n.-5+10278_-5+10279insT...
ENST00000672281.1:n.193+2954_193+2955insT
ENST00000673248.1:c.-127+10082_-127+10083insT ENSP00000500601.1:n.-127+10082_-127+10083...
ENST00000673360.1:c.-5+10082_-5+10083insT ENSP00000500360.1:n.-5+10082_-5+10083insT...
ENST00000673487.1:c.-5+10082_-5+10083insT ENSP00000500943.1:n.-5+10082_-5+10083insT...
ENST00000460945.5:n.169+10278_169+10279insT
ENST00000495360.5:c.-5+10082_-5+10083insT ENSP00000419623.1:n.-5+10082_-5+10083insT...
XM_011517936.1:c.-264+10301_-264+10302insT XP_011516238.1:n.-264+10301_-264+10302ins...
XM_011517937.1:c.-222+10278_-222+10279insT XP_011516239.1:n.-222+10278_-222+10279ins...
XM_017014837.2:c.-5+10082_-5+10083insT XP_016870326.1:n.-5+10082_-5+10083insT
XM_024447575.1:c.-5+10082_-5+10083insT XP_024303343.1:n.-5+10082_-5+10083insT
XM_024447576.1:c.-5+10278_-5+10279insT XP_024303344.1:n.-5+10278_-5+10279insT
XM_024447577.1:c.-5+10301_-5+10302insT XP_024303345.1:n.-5+10301_-5+10302insT
XM_024447579.1:c.-5+10082_-5+10083insT XP_024303347.1:n.-5+10082_-5+10083insT
XM_024447580.1:c.-5+10301_-5+10302insT XP_024303348.1:n.-5+10301_-5+10302insT
XM_024447581.1:c.-264+10082_-264+10083insT XP_024303349.1:n.-264+10082_-264+10083ins...
XM_024447582.1:c.-264+10278_-264+10279insT XP_024303350.1:n.-264+10278_-264+10279ins...
NM_001368995.1:c.-5+10278_-5+10279insT NP_001355924.1:n.-5+10278_-5+10279insT
NM_001368996.1:c.-5+10301_-5+10302insT NP_001355925.1:n.-5+10301_-5+10302insT
NM_001368997.1:c.-5+10082_-5+10083insT NP_001355926.1:n.-5+10082_-5+10083insT
NM_001368999.1:c.-5+10082_-5+10083insT NP_001355928.1:n.-5+10082_-5+10083insT
NM_001369000.1:c.-5+10082_-5+10083insT NP_001355929.1:n.-5+10082_-5+10083insT
NM_001369001.1:c.-5+10301_-5+10302insT NP_001355930.1:n.-5+10301_-5+10302insT
NM_001369002.1:c.-264+10278_-264+10279insT NP_001355931.1:n.-264+10278_-264+10279ins...
NM_001369003.1:c.-264+10082_-264+10083insT NP_001355932.1:n.-264+10082_-264+10083ins...
NR_160922.1:n.317+10082_317+10083insT
NR_160923.1:n.121+10278_121+10279insT
NR_160924.1:n.121+10278_121+10279insT
NR_160925.1:n.317+10082_317+10083insT
NR_160926.1:n.121+10278_121+10279insT
NR_160927.1:n.317+10082_317+10083insT
NR_160928.1:n.317+10082_317+10083insT
NR_160929.1:n.121+10278_121+10279insT