Canonical Allele Identifier: CA2646597647

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837912_92837913insTTTTAGT , CM000663.2:g.92837912_92837913insTTTTAGT GRCh38
NC_000001.10:g.93303469_93303470insTTTTAGT , CM000663.1:g.93303469_93303470insTTTTAGT GRCh37
NC_000001.9:g.93076057_93076058insTTTTAGT NCBI36
NG_011779.1:g.10876_10877insTTTTAGT
NG_033051.1:g.128610_128611insACTAAAA
NG_011779.2:g.10927_10928insTTTTAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+279_705+280insTTTTAGT (RPL5) MANE Select ENSP00000359345.2:n.705+279_705+280insTTTTAGT
ENST00000645119.1:c.325-2639_325-2638insTTTTAGT (RPL5) ENSP00000493811.1:n.325-2639_325-2638insTTTTAGT
ENST00000645300.1:c.555+279_555+280insTTTTAGT (RPL5) ENSP00000495589.1:n.555+279_555+280insTTTTAGT
ENST00000370321.7:c.705+279_705+280insTTTTAGT (RPL5) ENSP00000359345.2:n.705+279_705+280insTTTTAGT
ENST00000497519.1:n.1024+279_1024+280insTTTTAGT (RPL5)
ENST00000615519.4:c.475-4879_475-4878insACTAAAA (DIPK1A) ENSP00000483279.1:n.475-4879_475-4878insACTAAAA
NM_000969.3:c.705+279_705+280insTTTTAGT (RPL5) NP_000960.2:n.705+279_705+280insTTTTAGT
NM_001252273.1:c.475-4879_475-4878insACTAAAA (DIPK1A) NP_001239202.1:n.475-4879_475-4878insACTAAAA
NM_000969.5:c.705+279_705+280insTTTTAGT (RPL5) MANE Select NP_000960.2:n.705+279_705+280insTTTTAGT
NR_146333.1:n.764+279_764+280insTTTTAGT (RPL5)
NM_001252273.2:c.475-4879_475-4878insACTAAAA (DIPK1A) NP_001239202.1:n.475-4879_475-4878insACTAAAA