Canonical Allele Identifier: CA1180934244

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837715_92837720delinsCTTATA , CM000663.2:g.92837715_92837720delinsCTTATA GRCh38
NC_000001.10:g.93303272_93303277delinsCTTATA , CM000663.1:g.93303272_93303277delinsCTTATA GRCh37
NC_000001.9:g.93075860_93075865delinsCTTATA NCBI36
NG_011779.1:g.10679_10684delinsCTTATA
NG_033051.1:g.128803_128808delinsTATAAG
NG_011779.2:g.10730_10735delinsCTTATA

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+82_705+87delinsCTTATA (RPL5) MANE Select ENSP00000359345.2:n.705+82_705+87delinsCTTATA
ENST00000645119.1:c.324+2802_324+2807delinsCTTATA (RPL5) ENSP00000493811.1:n.324+2802_324+2807delinsCTTATA
ENST00000645300.1:c.555+82_555+87delinsCTTATA (RPL5) ENSP00000495589.1:n.555+82_555+87delinsCTTATA
ENST00000645908.1:n.521_526delinsCTTATA (RPL5)
ENST00000370321.7:c.705+82_705+87delinsCTTATA (RPL5) ENSP00000359345.2:n.705+82_705+87delinsCTTATA
ENST00000497519.1:n.1024+82_1024+87delinsCTTATA (RPL5)
ENST00000615519.4:c.475-4686_475-4681delinsTATAAG (DIPK1A) ENSP00000483279.1:n.475-4686_475-4681delinsTATAAG
NM_000969.3:c.705+82_705+87delinsCTTATA (RPL5) NP_000960.2:n.705+82_705+87delinsCTTATA
NM_001252273.1:c.475-4686_475-4681delinsTATAAG (DIPK1A) NP_001239202.1:n.475-4686_475-4681delinsTATAAG
NM_000969.5:c.705+82_705+87delinsCTTATA (RPL5) MANE Select NP_000960.2:n.705+82_705+87delinsCTTATA
NR_146333.1:n.764+82_764+87delinsCTTATA (RPL5)
NM_001252273.2:c.475-4686_475-4681delinsTATAAG (DIPK1A) NP_001239202.1:n.475-4686_475-4681delinsTATAAG