Canonical Allele Identifier: CA2646597506

Linked Data

gnomAD v4: 1-92837781-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837781A>G , CM000663.2:g.92837781A>G GRCh38
NC_000001.10:g.93303338A>G , CM000663.1:g.93303338A>G GRCh37
NC_000001.9:g.93075926A>G NCBI36
NG_011779.1:g.10745A>G
NG_033051.1:g.128742T>C
NG_011779.2:g.10796A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+148A>G (RPL5) MANE Select ENSP00000359345.2:n.705+148A>G
ENST00000645119.1:c.325-2770A>G (RPL5) ENSP00000493811.1:n.325-2770A>G
ENST00000645300.1:c.555+148A>G (RPL5) ENSP00000495589.1:n.555+148A>G
ENST00000645908.1:n.587A>G (RPL5)
ENST00000370321.7:c.705+148A>G (RPL5) ENSP00000359345.2:n.705+148A>G
ENST00000497519.1:n.1024+148A>G (RPL5)
ENST00000615519.4:c.475-4747T>C (DIPK1A) ENSP00000483279.1:n.475-4747T>C
NM_000969.3:c.705+148A>G (RPL5) NP_000960.2:n.705+148A>G
NM_001252273.1:c.475-4747T>C (DIPK1A) NP_001239202.1:n.475-4747T>C
NM_000969.5:c.705+148A>G (RPL5) MANE Select NP_000960.2:n.705+148A>G
NR_146333.1:n.764+148A>G (RPL5)
NM_001252273.2:c.475-4747T>C (DIPK1A) NP_001239202.1:n.475-4747T>C