Canonical Allele Identifier: CA1180934312

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837884_92837889delinsCTGCTT , CM000663.2:g.92837884_92837889delinsCTGCTT GRCh38
NC_000001.10:g.93303441_93303446delinsCTGCTT , CM000663.1:g.93303441_93303446delinsCTGCTT GRCh37
NC_000001.9:g.93076029_93076034delinsCTGCTT NCBI36
NG_011779.1:g.10848_10853delinsCTGCTT
NG_033051.1:g.128634_128639delinsAAGCAG
NG_011779.2:g.10899_10904delinsCTGCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+251_705+256delinsCTGCTT (RPL5) MANE Select ENSP00000359345.2:n.705+251_705+256delinsCTGCTT
ENST00000645119.1:c.325-2667_325-2662delinsCTGCTT (RPL5) ENSP00000493811.1:n.325-2667_325-2662delinsCTGCTT
ENST00000645300.1:c.555+251_555+256delinsCTGCTT (RPL5) ENSP00000495589.1:n.555+251_555+256delinsCTGCTT
ENST00000370321.7:c.705+251_705+256delinsCTGCTT (RPL5) ENSP00000359345.2:n.705+251_705+256delinsCTGCTT
ENST00000497519.1:n.1024+251_1024+256delinsCTGCTT (RPL5)
ENST00000615519.4:c.475-4855_475-4850delinsAAGCAG (DIPK1A) ENSP00000483279.1:n.475-4855_475-4850delinsAAGCAG
NM_000969.3:c.705+251_705+256delinsCTGCTT (RPL5) NP_000960.2:n.705+251_705+256delinsCTGCTT
NM_001252273.1:c.475-4855_475-4850delinsAAGCAG (DIPK1A) NP_001239202.1:n.475-4855_475-4850delinsAAGCAG
NM_000969.5:c.705+251_705+256delinsCTGCTT (RPL5) MANE Select NP_000960.2:n.705+251_705+256delinsCTGCTT
NR_146333.1:n.764+251_764+256delinsCTGCTT (RPL5)
NM_001252273.2:c.475-4855_475-4850delinsAAGCAG (DIPK1A) NP_001239202.1:n.475-4855_475-4850delinsAAGCAG