Canonical Allele Identifier: CA341243059

Gene: RPL5 DIPK1A

Linked Data

• MyVariant Identifiers: chr1:g.93303142C>G (hg19) ; chr1:g.92837585C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92837585C>G , CM000663.2:g.92837585C>G	GRCh38
NC_000001.10:g.93303142C>G , CM000663.1:g.93303142C>G	GRCh37
NC_000001.9:g.93075730C>G	NCBI36
NG_011779.1:g.10549C>G
NG_033051.1:g.128938G>C
NG_011779.2:g.10600C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370321.8:c.657C>G (RPL5) MANE Select	ENSP00000359345.2:p.Tyr219Ter
ENST00000645119.1:c.324+2672C>G (RPL5)	ENSP00000493811.1:n.324+2672C>G
ENST00000645300.1:c.507C>G (RPL5)	ENSP00000495589.1:p.Tyr169Ter
ENST00000645908.1:n.391C>G (RPL5)
ENST00000370321.7:c.657C>G (RPL5)	ENSP00000359345.2:p.Tyr219Ter
ENST00000497519.1:n.976C>G (RPL5)
ENST00000615519.4:c.475-4551G>C (DIPK1A)	ENSP00000483279.1:n.475-4551G>C
NM_000969.3:c.657C>G (RPL5)	NP_000960.2:p.Tyr219Ter
NM_001252273.1:c.475-4551G>C (DIPK1A)	NP_001239202.1:n.475-4551G>C
NM_000969.5:c.657C>G (RPL5) MANE Select	NP_000960.2:p.Tyr219Ter
NR_146333.1:n.716C>G (RPL5)
NM_001252273.2:c.475-4551G>C (DIPK1A)	NP_001239202.1:n.475-4551G>C