Canonical Allele Identifier: CA1180934221

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837665_92837667delinsGTT , CM000663.2:g.92837665_92837667delinsGTT GRCh38
NC_000001.10:g.93303222_93303224delinsGTT , CM000663.1:g.93303222_93303224delinsGTT GRCh37
NC_000001.9:g.93075810_93075812delinsGTT NCBI36
NG_011779.1:g.10629_10631delinsGTT
NG_033051.1:g.128856_128858delinsAAC
NG_011779.2:g.10680_10682delinsGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+32_705+34delinsGTT (RPL5) MANE Select ENSP00000359345.2:n.705+32_705+34delinsGTT
ENST00000645119.1:c.324+2752_324+2754delinsGTT (RPL5) ENSP00000493811.1:n.324+2752_324+2754delinsGTT
ENST00000645300.1:c.555+32_555+34delinsGTT (RPL5) ENSP00000495589.1:n.555+32_555+34delinsGTT
ENST00000645908.1:n.471_473delinsGTT (RPL5)
ENST00000370321.7:c.705+32_705+34delinsGTT (RPL5) ENSP00000359345.2:n.705+32_705+34delinsGTT
ENST00000497519.1:n.1024+32_1024+34delinsGTT (RPL5)
ENST00000615519.4:c.475-4633_475-4631delinsAAC (DIPK1A) ENSP00000483279.1:n.475-4633_475-4631delinsAAC
NM_000969.3:c.705+32_705+34delinsGTT (RPL5) NP_000960.2:n.705+32_705+34delinsGTT
NM_001252273.1:c.475-4633_475-4631delinsAAC (DIPK1A) NP_001239202.1:n.475-4633_475-4631delinsAAC
NM_000969.5:c.705+32_705+34delinsGTT (RPL5) MANE Select NP_000960.2:n.705+32_705+34delinsGTT
NR_146333.1:n.764+32_764+34delinsGTT (RPL5)
NM_001252273.2:c.475-4633_475-4631delinsAAC (DIPK1A) NP_001239202.1:n.475-4633_475-4631delinsAAC