Canonical Allele Identifier: CA2549763002

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837063_92837065del , CM000663.2:g.92837063_92837065del GRCh38
NC_000001.10:g.93302620_93302622del , CM000663.1:g.93302620_93302622del GRCh37
NC_000001.9:g.93075208_93075210del NCBI36
NG_011779.1:g.10027_10029del
NG_033051.1:g.129460_129462del
NG_011779.2:g.10078_10080del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-393_528-391del (RPL5) MANE Select ENSP00000359345.2:n.528-393_528-391del
ENST00000645119.1:c.324+2150_324+2152del (RPL5) ENSP00000493811.1:n.324+2150_324+2152del
ENST00000645300.1:c.378-393_378-391del (RPL5) ENSP00000495589.1:n.378-393_378-391del
ENST00000645908.1:n.262-393_262-391del (RPL5)
ENST00000315741.5:c.378-393_378-391del (RPL5) ENSP00000359338.2:n.378-393_378-391del
ENST00000370321.7:c.528-393_528-391del (RPL5) ENSP00000359345.2:n.528-393_528-391del
ENST00000497519.1:n.454_456del (RPL5)
ENST00000615519.4:c.475-4029_475-4027del (DIPK1A) ENSP00000483279.1:n.475-4029_475-4027del
NM_000969.3:c.528-393_528-391del (RPL5) NP_000960.2:n.528-393_528-391del
NM_001252273.1:c.475-4029_475-4027del (DIPK1A) NP_001239202.1:n.475-4029_475-4027del
NM_000969.5:c.528-393_528-391del (RPL5) MANE Select NP_000960.2:n.528-393_528-391del
NR_146333.1:n.587-393_587-391del (RPL5)
NM_001252273.2:c.475-4029_475-4027del (DIPK1A) NP_001239202.1:n.475-4029_475-4027del