Canonical Allele Identifier: CA1180933966

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837039_92837040delinsTG , CM000663.2:g.92837039_92837040delinsTG GRCh38
NC_000001.10:g.93302596_93302597delinsTG , CM000663.1:g.93302596_93302597delinsTG GRCh37
NC_000001.9:g.93075184_93075185delinsTG NCBI36
NG_011779.1:g.10003_10004delinsTG
NG_033051.1:g.129483_129484delinsCA
NG_011779.2:g.10054_10055delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-417_528-416delinsTG (RPL5) MANE Select ENSP00000359345.2:n.528-417_528-416delinsTG
ENST00000645119.1:c.324+2126_324+2127delinsTG (RPL5) ENSP00000493811.1:n.324+2126_324+2127delinsTG
ENST00000645300.1:c.378-417_378-416delinsTG (RPL5) ENSP00000495589.1:n.378-417_378-416delinsTG
ENST00000645908.1:n.262-417_262-416delinsTG (RPL5)
ENST00000315741.5:c.378-417_378-416delinsTG (RPL5) ENSP00000359338.2:n.378-417_378-416delinsTG
ENST00000370321.7:c.528-417_528-416delinsTG (RPL5) ENSP00000359345.2:n.528-417_528-416delinsTG
ENST00000497519.1:n.430_431delinsTG (RPL5)
ENST00000615519.4:c.475-4006_475-4005delinsCA (DIPK1A) ENSP00000483279.1:n.475-4006_475-4005delinsCA
NM_000969.3:c.528-417_528-416delinsTG (RPL5) NP_000960.2:n.528-417_528-416delinsTG
NM_001252273.1:c.475-4006_475-4005delinsCA (DIPK1A) NP_001239202.1:n.475-4006_475-4005delinsCA
NM_000969.5:c.528-417_528-416delinsTG (RPL5) MANE Select NP_000960.2:n.528-417_528-416delinsTG
NR_146333.1:n.587-417_587-416delinsTG (RPL5)
NM_001252273.2:c.475-4006_475-4005delinsCA (DIPK1A) NP_001239202.1:n.475-4006_475-4005delinsCA