Canonical Allele Identifier: CA341242779

Gene: RPL5 DIPK1A

Linked Data

• MyVariant Identifiers: chr1:g.93303024T>A (hg19) ; chr1:g.92837467T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92837467T>A , CM000663.2:g.92837467T>A	GRCh38
NC_000001.10:g.93303024T>A , CM000663.1:g.93303024T>A	GRCh37
NC_000001.9:g.93075612T>A	NCBI36
NG_011779.1:g.10431T>A
NG_033051.1:g.129056A>T
NG_011779.2:g.10482T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000370321.8:c.539T>A (RPL5) MANE Select	ENSP00000359345.2:p.Phe180Tyr
ENST00000645119.1:c.324+2554T>A (RPL5)	ENSP00000493811.1:n.324+2554T>A
ENST00000645300.1:c.389T>A (RPL5)	ENSP00000495589.1:p.Phe130Tyr
ENST00000645908.1:n.273T>A (RPL5)
ENST00000315741.5:c.389T>A (RPL5)	ENSP00000359338.2:p.Phe130Tyr
ENST00000370321.7:c.539T>A (RPL5)	ENSP00000359345.2:p.Phe180Tyr
ENST00000497519.1:n.858T>A (RPL5)
ENST00000615519.4:c.475-4433A>T (DIPK1A)	ENSP00000483279.1:n.475-4433A>T
NM_000969.3:c.539T>A (RPL5)	NP_000960.2:p.Phe180Tyr
NM_001252273.1:c.475-4433A>T (DIPK1A)	NP_001239202.1:n.475-4433A>T
NM_000969.5:c.539T>A (RPL5) MANE Select	NP_000960.2:p.Phe180Tyr
NR_146333.1:n.598T>A (RPL5)
NM_001252273.2:c.475-4433A>T (DIPK1A)	NP_001239202.1:n.475-4433A>T