Canonical Allele Identifier: CA916235789

Linked Data

dbSNP Id: rs1571030957

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837098_92837099del , CM000663.2:g.92837098_92837099del GRCh38
NC_000001.10:g.93302655_93302656del , CM000663.1:g.93302655_93302656del GRCh37
NC_000001.9:g.93075243_93075244del NCBI36
NG_011779.1:g.10062_10063del
NG_033051.1:g.129426_129427del
NG_011779.2:g.10113_10114del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.528-358_528-357del (RPL5) MANE Select ENSP00000359345.2:n.528-358_528-357del
ENST00000645119.1:c.324+2185_324+2186del (RPL5) ENSP00000493811.1:n.324+2185_324+2186del
ENST00000645300.1:c.378-358_378-357del (RPL5) ENSP00000495589.1:n.378-358_378-357del
ENST00000645908.1:n.262-358_262-357del (RPL5)
ENST00000315741.5:c.378-358_378-357del (RPL5) ENSP00000359338.2:n.378-358_378-357del
ENST00000370321.7:c.528-358_528-357del (RPL5) ENSP00000359345.2:n.528-358_528-357del
ENST00000497519.1:n.489_490del (RPL5)
ENST00000615519.4:c.475-4063_475-4062del (DIPK1A) ENSP00000483279.1:n.475-4063_475-4062del
NM_000969.3:c.528-358_528-357del (RPL5) NP_000960.2:n.528-358_528-357del
NM_001252273.1:c.475-4063_475-4062del (DIPK1A) NP_001239202.1:n.475-4063_475-4062del
NM_000969.5:c.528-358_528-357del (RPL5) MANE Select NP_000960.2:n.528-358_528-357del
NR_146333.1:n.587-358_587-357del (RPL5)
NM_001252273.2:c.475-4063_475-4062del (DIPK1A) NP_001239202.1:n.475-4063_475-4062del