Canonical Allele Identifier: CA341242788

Gene: RPL5 DIPK1A

Linked Data

• MyVariant Identifiers: chr1:g.93303027C>G (hg19) ; chr1:g.92837470C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92837470C>G , CM000663.2:g.92837470C>G	GRCh38
NC_000001.10:g.93303027C>G , CM000663.1:g.93303027C>G	GRCh37
NC_000001.9:g.93075615C>G	NCBI36
NG_011779.1:g.10434C>G
NG_033051.1:g.129053G>C
NG_011779.2:g.10485C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000370321.8:c.542C>G (RPL5) MANE Select	ENSP00000359345.2:p.Pro181Arg
ENST00000645119.1:c.324+2557C>G (RPL5)	ENSP00000493811.1:n.324+2557C>G
ENST00000645300.1:c.392C>G (RPL5)	ENSP00000495589.1:p.Pro131Arg
ENST00000645908.1:n.276C>G (RPL5)
ENST00000370321.7:c.542C>G (RPL5)	ENSP00000359345.2:p.Pro181Arg
ENST00000497519.1:n.861C>G (RPL5)
ENST00000615519.4:c.475-4436G>C (DIPK1A)	ENSP00000483279.1:n.475-4436G>C
NM_000969.3:c.542C>G (RPL5)	NP_000960.2:p.Pro181Arg
NM_001252273.1:c.475-4436G>C (DIPK1A)	NP_001239202.1:n.475-4436G>C
NM_000969.5:c.542C>G (RPL5) MANE Select	NP_000960.2:p.Pro181Arg
NR_146333.1:n.601C>G (RPL5)
NM_001252273.2:c.475-4436G>C (DIPK1A)	NP_001239202.1:n.475-4436G>C