Canonical Allele Identifier: CA1180934315

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837886_92837887delinsGC , CM000663.2:g.92837886_92837887delinsGC GRCh38
NC_000001.10:g.93303443_93303444delinsGC , CM000663.1:g.93303443_93303444delinsGC GRCh37
NC_000001.9:g.93076031_93076032delinsGC NCBI36
NG_011779.1:g.10850_10851delinsGC
NG_033051.1:g.128636_128637delinsGC
NG_011779.2:g.10901_10902delinsGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+253_705+254delinsGC (RPL5) MANE Select ENSP00000359345.2:n.705+253_705+254delinsGC
ENST00000645119.1:c.325-2665_325-2664delinsGC (RPL5) ENSP00000493811.1:n.325-2665_325-2664delinsGC
ENST00000645300.1:c.555+253_555+254delinsGC (RPL5) ENSP00000495589.1:n.555+253_555+254delinsGC
ENST00000370321.7:c.705+253_705+254delinsGC (RPL5) ENSP00000359345.2:n.705+253_705+254delinsGC
ENST00000497519.1:n.1024+253_1024+254delinsGC (RPL5)
ENST00000615519.4:c.475-4853_475-4852delinsGC (DIPK1A) ENSP00000483279.1:n.475-4853_475-4852delinsGC
NM_000969.3:c.705+253_705+254delinsGC (RPL5) NP_000960.2:n.705+253_705+254delinsGC
NM_001252273.1:c.475-4853_475-4852delinsGC (DIPK1A) NP_001239202.1:n.475-4853_475-4852delinsGC
NM_000969.5:c.705+253_705+254delinsGC (RPL5) MANE Select NP_000960.2:n.705+253_705+254delinsGC
NR_146333.1:n.764+253_764+254delinsGC (RPL5)
NM_001252273.2:c.475-4853_475-4852delinsGC (DIPK1A) NP_001239202.1:n.475-4853_475-4852delinsGC