Canonical Allele Identifier: CA418788782

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92833603C>T , CM000663.2:g.92833603C>T GRCh38
NC_000001.10:g.93299160C>T , CM000663.1:g.93299160C>T GRCh37
NC_000001.9:g.93071748C>T NCBI36
NG_011779.1:g.6567C>T
NG_033051.1:g.132920G>A
NG_011779.2:g.6618C>T

Transcript Alleles

HGVS Amino-acid Change
NM_000969.5:c.132C>T (RPL5) MANE Select NP_000960.2:p.Tyr44=
ENST00000370321.8:c.132C>T (RPL5) MANE Select ENSP00000359345.2:p.Tyr44=
NM_000969.3:c.132C>T (RPL5) NP_000960.2:p.Tyr44=
NM_001252273.1:c.475-569G>A (DIPK1A) NP_001239202.1:n.475-569G>A
NM_001252273.2:c.475-569G>A (DIPK1A) NP_001239202.1:n.475-569G>A
NR_146333.1:n.261C>T (RPL5)
ENST00000315741.5:c.-19C>T (RPL5) ENSP00000359338.2:n.-19C>T
ENST00000370321.7:c.132C>T (RPL5) ENSP00000359345.2:p.Tyr44=
ENST00000461952.1:n.842C>T (RPL5)
ENST00000470843.5:c.132C>T (RPL5) ENSP00000473675.1:p.Tyr44=
ENST00000615519.4:c.475-569G>A (DIPK1A) ENSP00000483279.1:n.475-569G>A
ENST00000645119.1:c.132C>T (RPL5) ENSP00000493811.1:p.Tyr44=
ENST00000645300.1:c.-19C>T (RPL5) ENSP00000495589.1:n.-19C>T
ENST00000646852.1:n.161C>T (RPL5)