Canonical Allele Identifier: CA1180934318

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837890_92837894delinsTGTTG , CM000663.2:g.92837890_92837894delinsTGTTG GRCh38
NC_000001.10:g.93303447_93303451delinsTGTTG , CM000663.1:g.93303447_93303451delinsTGTTG GRCh37
NC_000001.9:g.93076035_93076039delinsTGTTG NCBI36
NG_011779.1:g.10854_10858delinsTGTTG
NG_033051.1:g.128629_128633delinsCAACA
NG_011779.2:g.10905_10909delinsTGTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+257_705+261delinsTGTTG (RPL5) MANE Select ENSP00000359345.2:n.705+257_705+261delinsTGTTG
ENST00000645119.1:c.325-2661_325-2657delinsTGTTG (RPL5) ENSP00000493811.1:n.325-2661_325-2657delinsTGTTG
ENST00000645300.1:c.555+257_555+261delinsTGTTG (RPL5) ENSP00000495589.1:n.555+257_555+261delinsTGTTG
ENST00000370321.7:c.705+257_705+261delinsTGTTG (RPL5) ENSP00000359345.2:n.705+257_705+261delinsTGTTG
ENST00000497519.1:n.1024+257_1024+261delinsTGTTG (RPL5)
ENST00000615519.4:c.475-4860_475-4856delinsCAACA (DIPK1A) ENSP00000483279.1:n.475-4860_475-4856delinsCAACA
NM_000969.3:c.705+257_705+261delinsTGTTG (RPL5) NP_000960.2:n.705+257_705+261delinsTGTTG
NM_001252273.1:c.475-4860_475-4856delinsCAACA (DIPK1A) NP_001239202.1:n.475-4860_475-4856delinsCAACA
NM_000969.5:c.705+257_705+261delinsTGTTG (RPL5) MANE Select NP_000960.2:n.705+257_705+261delinsTGTTG
NR_146333.1:n.764+257_764+261delinsTGTTG (RPL5)
NM_001252273.2:c.475-4860_475-4856delinsCAACA (DIPK1A) NP_001239202.1:n.475-4860_475-4856delinsCAACA