Canonical Allele Identifier: CA2646597459

Linked Data

gnomAD v4: 1-92837703-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837703G>C , CM000663.2:g.92837703G>C GRCh38
NC_000001.10:g.93303260G>C , CM000663.1:g.93303260G>C GRCh37
NC_000001.9:g.93075848G>C NCBI36
NG_011779.1:g.10667G>C
NG_033051.1:g.128820C>G
NG_011779.2:g.10718G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+70G>C (RPL5) MANE Select ENSP00000359345.2:n.705+70G>C
ENST00000645119.1:c.324+2790G>C (RPL5) ENSP00000493811.1:n.324+2790G>C
ENST00000645300.1:c.555+70G>C (RPL5) ENSP00000495589.1:n.555+70G>C
ENST00000645908.1:n.509G>C (RPL5)
ENST00000370321.7:c.705+70G>C (RPL5) ENSP00000359345.2:n.705+70G>C
ENST00000497519.1:n.1024+70G>C (RPL5)
ENST00000615519.4:c.475-4669C>G (DIPK1A) ENSP00000483279.1:n.475-4669C>G
NM_000969.3:c.705+70G>C (RPL5) NP_000960.2:n.705+70G>C
NM_001252273.1:c.475-4669C>G (DIPK1A) NP_001239202.1:n.475-4669C>G
NM_000969.5:c.705+70G>C (RPL5) MANE Select NP_000960.2:n.705+70G>C
NR_146333.1:n.764+70G>C (RPL5)
NM_001252273.2:c.475-4669C>G (DIPK1A) NP_001239202.1:n.475-4669C>G