Canonical Allele Identifier: CA26757199

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833927G>C , CM000663.2:g.92833927G>C GRCh38
NC_000001.10:g.93299484G>C , CM000663.1:g.93299484G>C GRCh37
NC_000001.9:g.93072072G>C NCBI36
NG_011779.1:g.6891G>C
NG_033051.1:g.132596C>G
NG_011779.2:g.6942G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.189+267G>C (RPL5) MANE Select ENSP00000359345.2:n.189+267G>C
ENST00000645119.1:c.189+267G>C (RPL5) ENSP00000493811.1:n.189+267G>C
ENST00000645300.1:c.39+267G>C (RPL5) ENSP00000495589.1:n.39+267G>C
ENST00000646852.1:n.218+267G>C (RPL5)
ENST00000315741.5:c.39+267G>C (RPL5) ENSP00000359338.2:n.39+267G>C
ENST00000370321.7:c.189+267G>C (RPL5) ENSP00000359345.2:n.189+267G>C
ENST00000461952.1:n.899+267G>C (RPL5)
ENST00000470843.5:c.*129G>C (RPL5) ENSP00000473675.1:n.*129G>C
ENST00000615519.4:c.475-893C>G (DIPK1A) ENSP00000483279.1:n.475-893C>G
NM_000969.3:c.189+267G>C (RPL5) NP_000960.2:n.189+267G>C
NM_001252273.1:c.475-893C>G (DIPK1A) NP_001239202.1:n.475-893C>G
NM_000969.5:c.189+267G>C (RPL5) MANE Select NP_000960.2:n.189+267G>C
NR_146333.1:n.318+267G>C (RPL5)
NM_001252273.2:c.475-893C>G (DIPK1A) NP_001239202.1:n.475-893C>G