Canonical Allele Identifier: CA1180934246

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837716_92837718delinsTTA , CM000663.2:g.92837716_92837718delinsTTA GRCh38
NC_000001.10:g.93303273_93303275delinsTTA , CM000663.1:g.93303273_93303275delinsTTA GRCh37
NC_000001.9:g.93075861_93075863delinsTTA NCBI36
NG_011779.1:g.10680_10682delinsTTA
NG_033051.1:g.128805_128807delinsTAA
NG_011779.2:g.10731_10733delinsTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+83_705+85delinsTTA (RPL5) MANE Select ENSP00000359345.2:n.705+83_705+85delinsTTA
ENST00000645119.1:c.324+2803_324+2805delinsTTA (RPL5) ENSP00000493811.1:n.324+2803_324+2805delinsTTA
ENST00000645300.1:c.555+83_555+85delinsTTA (RPL5) ENSP00000495589.1:n.555+83_555+85delinsTTA
ENST00000645908.1:n.522_524delinsTTA (RPL5)
ENST00000370321.7:c.705+83_705+85delinsTTA (RPL5) ENSP00000359345.2:n.705+83_705+85delinsTTA
ENST00000497519.1:n.1024+83_1024+85delinsTTA (RPL5)
ENST00000615519.4:c.475-4684_475-4682delinsTAA (DIPK1A) ENSP00000483279.1:n.475-4684_475-4682delinsTAA
NM_000969.3:c.705+83_705+85delinsTTA (RPL5) NP_000960.2:n.705+83_705+85delinsTTA
NM_001252273.1:c.475-4684_475-4682delinsTAA (DIPK1A) NP_001239202.1:n.475-4684_475-4682delinsTAA
NM_000969.5:c.705+83_705+85delinsTTA (RPL5) MANE Select NP_000960.2:n.705+83_705+85delinsTTA
NR_146333.1:n.764+83_764+85delinsTTA (RPL5)
NM_001252273.2:c.475-4684_475-4682delinsTAA (DIPK1A) NP_001239202.1:n.475-4684_475-4682delinsTAA