Canonical Allele Identifier: CA1180934314

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837886G= , CM000663.2:g.92837886G= GRCh38
NC_000001.10:g.93303443G= , CM000663.1:g.93303443G= GRCh37
NC_000001.9:g.93076031G= NCBI36
NG_011779.1:g.10850G=
NG_033051.1:g.128637C=
NG_011779.2:g.10901G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+253G= (RPL5) MANE Select ENSP00000359345.2:n.705+253G=
ENST00000645119.1:c.325-2665G= (RPL5) ENSP00000493811.1:n.325-2665G=
ENST00000645300.1:c.555+253G= (RPL5) ENSP00000495589.1:n.555+253G=
ENST00000370321.7:c.705+253G= (RPL5) ENSP00000359345.2:n.705+253G=
ENST00000497519.1:n.1024+253G= (RPL5)
ENST00000615519.4:c.475-4852C= (DIPK1A) ENSP00000483279.1:n.475-4852C=
NM_000969.3:c.705+253G= (RPL5) NP_000960.2:n.705+253G=
NM_001252273.1:c.475-4852C= (DIPK1A) NP_001239202.1:n.475-4852C=
NM_000969.5:c.705+253G= (RPL5) MANE Select NP_000960.2:n.705+253G=
NR_146333.1:n.764+253G= (RPL5)
NM_001252273.2:c.475-4852C= (DIPK1A) NP_001239202.1:n.475-4852C=