Canonical Allele Identifier: CA418789324

Linked Data

MyVariant Identifiers: chr1:g.93303046C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.92837489C>T , CM000663.2:g.92837489C>T GRCh38
NC_000001.10:g.93303046C>T , CM000663.1:g.93303046C>T GRCh37
NC_000001.9:g.93075634C>T NCBI36
NG_011779.1:g.10453C>T
NG_033051.1:g.129034G>A
NG_011779.2:g.10504C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000370321.8:c.561C>T (RPL5) MANE Select ENSP00000359345.2:p.Ser187=
ENST00000645119.1:c.324+2576C>T (RPL5) ENSP00000493811.1:n.324+2576C>T
ENST00000645300.1:c.411C>T (RPL5) ENSP00000495589.1:p.Ser137=
ENST00000645908.1:n.295C>T (RPL5)
ENST00000370321.7:c.561C>T (RPL5) ENSP00000359345.2:p.Ser187=
ENST00000497519.1:n.880C>T (RPL5)
ENST00000615519.4:c.475-4455G>A (DIPK1A) ENSP00000483279.1:n.475-4455G>A
NM_000969.3:c.561C>T (RPL5) NP_000960.2:p.Ser187=
NM_001252273.1:c.475-4455G>A (DIPK1A) NP_001239202.1:n.475-4455G>A
NM_000969.5:c.561C>T (RPL5) MANE Select NP_000960.2:p.Ser187=
NR_146333.1:n.620C>T (RPL5)
NM_001252273.2:c.475-4455G>A (DIPK1A) NP_001239202.1:n.475-4455G>A