Canonical Allele Identifier: CA418789333

Gene: RPL5 DIPK1A

Linked Data

• MyVariant Identifiers: chr1:g.93303067A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.92837510A>G , CM000663.2:g.92837510A>G	GRCh38
NC_000001.10:g.93303067A>G , CM000663.1:g.93303067A>G	GRCh37
NC_000001.9:g.93075655A>G	NCBI36
NG_011779.1:g.10474A>G
NG_033051.1:g.129013T>C
NG_011779.2:g.10525A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370321.8:c.582A>G (RPL5) MANE Select	ENSP00000359345.2:p.Val194=
ENST00000645119.1:c.324+2597A>G (RPL5)	ENSP00000493811.1:n.324+2597A>G
ENST00000645300.1:c.432A>G (RPL5)	ENSP00000495589.1:p.Val144=
ENST00000645908.1:n.316A>G (RPL5)
ENST00000370321.7:c.582A>G (RPL5)	ENSP00000359345.2:p.Val194=
ENST00000497519.1:n.901A>G (RPL5)
ENST00000615519.4:c.475-4476T>C (DIPK1A)	ENSP00000483279.1:n.475-4476T>C
NM_000969.3:c.582A>G (RPL5)	NP_000960.2:p.Val194=
NM_001252273.1:c.475-4476T>C (DIPK1A)	NP_001239202.1:n.475-4476T>C
NM_000969.5:c.582A>G (RPL5) MANE Select	NP_000960.2:p.Val194=
NR_146333.1:n.641A>G (RPL5)
NM_001252273.2:c.475-4476T>C (DIPK1A)	NP_001239202.1:n.475-4476T>C