Canonical Allele Identifier: CA418789345

Linked Data

MyVariant Identifiers: chr1:g.93303088C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837531C>G , CM000663.2:g.92837531C>G GRCh38
NC_000001.10:g.93303088C>G , CM000663.1:g.93303088C>G GRCh37
NC_000001.9:g.93075676C>G NCBI36
NG_011779.1:g.10495C>G
NG_033051.1:g.128992G>C
NG_011779.2:g.10546C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.603C>G (RPL5) MANE Select ENSP00000359345.2:p.Gly201=
ENST00000645119.1:c.324+2618C>G (RPL5) ENSP00000493811.1:n.324+2618C>G
ENST00000645300.1:c.453C>G (RPL5) ENSP00000495589.1:p.Gly151=
ENST00000645908.1:n.337C>G (RPL5)
ENST00000370321.7:c.603C>G (RPL5) ENSP00000359345.2:p.Gly201=
ENST00000497519.1:n.922C>G (RPL5)
ENST00000615519.4:c.475-4497G>C (DIPK1A) ENSP00000483279.1:n.475-4497G>C
NM_000969.3:c.603C>G (RPL5) NP_000960.2:p.Gly201=
NM_001252273.1:c.475-4497G>C (DIPK1A) NP_001239202.1:n.475-4497G>C
NM_000969.5:c.603C>G (RPL5) MANE Select NP_000960.2:p.Gly201=
NR_146333.1:n.662C>G (RPL5)
NM_001252273.2:c.475-4497G>C (DIPK1A) NP_001239202.1:n.475-4497G>C