Canonical Allele Identifier: CA26759814

Linked Data

dbSNP Id: rs549274227
gnomAD v4: 1-92837728-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837728G>C , CM000663.2:g.92837728G>C GRCh38
NC_000001.10:g.93303285G>C , CM000663.1:g.93303285G>C GRCh37
NC_000001.9:g.93075873G>C NCBI36
NG_011779.1:g.10692G>C
NG_033051.1:g.128795C>G
NG_011779.2:g.10743G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.705+95G>C (RPL5) MANE Select ENSP00000359345.2:n.705+95G>C
ENST00000645119.1:c.324+2815G>C (RPL5) ENSP00000493811.1:n.324+2815G>C
ENST00000645300.1:c.555+95G>C (RPL5) ENSP00000495589.1:n.555+95G>C
ENST00000645908.1:n.534G>C (RPL5)
ENST00000370321.7:c.705+95G>C (RPL5) ENSP00000359345.2:n.705+95G>C
ENST00000497519.1:n.1024+95G>C (RPL5)
ENST00000615519.4:c.475-4694C>G (DIPK1A) ENSP00000483279.1:n.475-4694C>G
NM_000969.3:c.705+95G>C (RPL5) NP_000960.2:n.705+95G>C
NM_001252273.1:c.475-4694C>G (DIPK1A) NP_001239202.1:n.475-4694C>G
NM_000969.5:c.705+95G>C (RPL5) MANE Select NP_000960.2:n.705+95G>C
NR_146333.1:n.764+95G>C (RPL5)
NM_001252273.2:c.475-4694C>G (DIPK1A) NP_001239202.1:n.475-4694C>G