Canonical Allele Identifier: CA341242850

Gene: RPL5 DIPK1A

Linked Data

• MyVariant Identifiers: chr1:g.93303054T>A (hg19) ; chr1:g.92837497T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92837497T>A , CM000663.2:g.92837497T>A	GRCh38
NC_000001.10:g.93303054T>A , CM000663.1:g.93303054T>A	GRCh37
NC_000001.9:g.93075642T>A	NCBI36
NG_011779.1:g.10461T>A
NG_033051.1:g.129026A>T
NG_011779.2:g.10512T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370321.8:c.569T>A (RPL5) MANE Select	ENSP00000359345.2:p.Phe190Tyr
ENST00000645119.1:c.324+2584T>A (RPL5)	ENSP00000493811.1:n.324+2584T>A
ENST00000645300.1:c.419T>A (RPL5)	ENSP00000495589.1:p.Phe140Tyr
ENST00000645908.1:n.303T>A (RPL5)
ENST00000370321.7:c.569T>A (RPL5)	ENSP00000359345.2:p.Phe190Tyr
ENST00000497519.1:n.888T>A (RPL5)
ENST00000615519.4:c.475-4463A>T (DIPK1A)	ENSP00000483279.1:n.475-4463A>T
NM_000969.3:c.569T>A (RPL5)	NP_000960.2:p.Phe190Tyr
NM_001252273.1:c.475-4463A>T (DIPK1A)	NP_001239202.1:n.475-4463A>T
NM_000969.5:c.569T>A (RPL5) MANE Select	NP_000960.2:p.Phe190Tyr
NR_146333.1:n.628T>A (RPL5)
NM_001252273.2:c.475-4463A>T (DIPK1A)	NP_001239202.1:n.475-4463A>T