Canonical Allele Identifier: CA1180934256

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837723_92837725delinsGGT , CM000663.2:g.92837723_92837725delinsGGT GRCh38
NC_000001.10:g.93303280_93303282delinsGGT , CM000663.1:g.93303280_93303282delinsGGT GRCh37
NC_000001.9:g.93075868_93075870delinsGGT NCBI36
NG_011779.1:g.10687_10689delinsGGT
NG_033051.1:g.128798_128800delinsACC
NG_011779.2:g.10738_10740delinsGGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+90_705+92delinsGGT (RPL5) MANE Select ENSP00000359345.2:n.705+90_705+92delinsGGT
ENST00000645119.1:c.324+2810_324+2812delinsGGT (RPL5) ENSP00000493811.1:n.324+2810_324+2812delinsGGT
ENST00000645300.1:c.555+90_555+92delinsGGT (RPL5) ENSP00000495589.1:n.555+90_555+92delinsGGT
ENST00000645908.1:n.529_531delinsGGT (RPL5)
ENST00000370321.7:c.705+90_705+92delinsGGT (RPL5) ENSP00000359345.2:n.705+90_705+92delinsGGT
ENST00000497519.1:n.1024+90_1024+92delinsGGT (RPL5)
ENST00000615519.4:c.475-4691_475-4689delinsACC (DIPK1A) ENSP00000483279.1:n.475-4691_475-4689delinsACC
NM_000969.3:c.705+90_705+92delinsGGT (RPL5) NP_000960.2:n.705+90_705+92delinsGGT
NM_001252273.1:c.475-4691_475-4689delinsACC (DIPK1A) NP_001239202.1:n.475-4691_475-4689delinsACC
NM_000969.5:c.705+90_705+92delinsGGT (RPL5) MANE Select NP_000960.2:n.705+90_705+92delinsGGT
NR_146333.1:n.764+90_764+92delinsGGT (RPL5)
NM_001252273.2:c.475-4691_475-4689delinsACC (DIPK1A) NP_001239202.1:n.475-4691_475-4689delinsACC