Canonical Allele Identifier: CA1180933952

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837018_92837019delinsCT , CM000663.2:g.92837018_92837019delinsCT GRCh38
NC_000001.10:g.93302575_93302576delinsCT , CM000663.1:g.93302575_93302576delinsCT GRCh37
NC_000001.9:g.93075163_93075164delinsCT NCBI36
NG_011779.1:g.9982_9983delinsCT
NG_033051.1:g.129504_129505delinsAG
NG_011779.2:g.10033_10034delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-438_528-437delinsCT (RPL5) MANE Select ENSP00000359345.2:n.528-438_528-437delinsCT
ENST00000645119.1:c.324+2105_324+2106delinsCT (RPL5) ENSP00000493811.1:n.324+2105_324+2106delinsCT
ENST00000645300.1:c.378-438_378-437delinsCT (RPL5) ENSP00000495589.1:n.378-438_378-437delinsCT
ENST00000645908.1:n.262-438_262-437delinsCT (RPL5)
ENST00000315741.5:c.378-438_378-437delinsCT (RPL5) ENSP00000359338.2:n.378-438_378-437delinsCT
ENST00000370321.7:c.528-438_528-437delinsCT (RPL5) ENSP00000359345.2:n.528-438_528-437delinsCT
ENST00000497519.1:n.409_410delinsCT (RPL5)
ENST00000615519.4:c.475-3985_475-3984delinsAG (DIPK1A) ENSP00000483279.1:n.475-3985_475-3984delinsAG
NM_000969.3:c.528-438_528-437delinsCT (RPL5) NP_000960.2:n.528-438_528-437delinsCT
NM_001252273.1:c.475-3985_475-3984delinsAG (DIPK1A) NP_001239202.1:n.475-3985_475-3984delinsAG
NM_000969.5:c.528-438_528-437delinsCT (RPL5) MANE Select NP_000960.2:n.528-438_528-437delinsCT
NR_146333.1:n.587-438_587-437delinsCT (RPL5)
NM_001252273.2:c.475-3985_475-3984delinsAG (DIPK1A) NP_001239202.1:n.475-3985_475-3984delinsAG