Canonical Allele Identifier: CA2646597452

Linked Data

gnomAD v4: 1-92837680-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837680T>G , CM000663.2:g.92837680T>G GRCh38
NC_000001.10:g.93303237T>G , CM000663.1:g.93303237T>G GRCh37
NC_000001.9:g.93075825T>G NCBI36
NG_011779.1:g.10644T>G
NG_033051.1:g.128843A>C
NG_011779.2:g.10695T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+47T>G (RPL5) MANE Select ENSP00000359345.2:n.705+47T>G
ENST00000645119.1:c.324+2767T>G (RPL5) ENSP00000493811.1:n.324+2767T>G
ENST00000645300.1:c.555+47T>G (RPL5) ENSP00000495589.1:n.555+47T>G
ENST00000645908.1:n.486T>G (RPL5)
ENST00000370321.7:c.705+47T>G (RPL5) ENSP00000359345.2:n.705+47T>G
ENST00000497519.1:n.1024+47T>G (RPL5)
ENST00000615519.4:c.475-4646A>C (DIPK1A) ENSP00000483279.1:n.475-4646A>C
NM_000969.3:c.705+47T>G (RPL5) NP_000960.2:n.705+47T>G
NM_001252273.1:c.475-4646A>C (DIPK1A) NP_001239202.1:n.475-4646A>C
NM_000969.5:c.705+47T>G (RPL5) MANE Select NP_000960.2:n.705+47T>G
NR_146333.1:n.764+47T>G (RPL5)
NM_001252273.2:c.475-4646A>C (DIPK1A) NP_001239202.1:n.475-4646A>C