Canonical Allele Identifier: CA1921524197

Gene: RPS24

Linked Data

• ClinVar Variation Id: 1045212
• ClinVar RCV Id: RCV001349581
• dbSNP Id: rs1847891159

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037266_78037268del , CM000672.2:g.78037266_78037268del	GRCh38
NC_000010.10:g.79797024_79797026del , CM000672.1:g.79797024_79797026del	GRCh37
NC_000010.9:g.79467030_79467032del	NCBI36
NG_012633.1:g.8507_8509del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.352_354del	ENSP00000354074.5:p.Arg118del
ENST00000372360.9:c.352_354del MANE Select	ENSP00000361435.4:p.Arg118del
ENST00000440692.6:c.352_354del	ENSP00000414321.1:p.Arg118del
ENST00000464716.6:c.352_354del	ENSP00000494231.1:p.Arg118del
ENST00000465692.2:n.363_365del
ENST00000476545.6:c.352_354del	ENSP00000494169.1:p.Arg118del
ENST00000478655.6:n.391_393del
ENST00000485708.7:n.391_393del
ENST00000613865.5:c.352_354del	ENSP00000478869.2:p.Arg118del
ENST00000645195.1:c.228_230del
ENST00000645440.1:c.352_354del	ENSP00000496738.1:p.Arg118del
ENST00000645698.1:n.380_382del
ENST00000360830.8:c.352_354del	ENSP00000354074.4:p.Arg118del
ENST00000372360.7:c.352_354del	ENSP00000361435.3:p.Arg118del
ENST00000435275.5:c.352_354del	ENSP00000415549.1:p.Arg118del
ENST00000440692.5:c.352_354del	ENSP00000414321.1:p.Arg118del
ENST00000464716.5:n.380_382del
ENST00000465692.1:n.349_351del
ENST00000476545.5:n.376_378del
ENST00000478655.5:n.391_393del
ENST00000482069.5:n.419_421del
ENST00000485708.6:n.410_412del
ENST00000613865.4:c.352_354del	ENSP00000478869.1:p.Arg118del
NM_001026.4:c.352_354del	NP_001017.1:p.Arg118del
NM_001142282.1:c.352_354del	NP_001135754.1:p.Arg118del
NM_001142283.1:c.352_354del	NP_001135755.1:p.Arg118del
NM_001142284.1:c.352_354del	NP_001135756.1:p.Arg118del
NM_001142285.1:c.352_354del	NP_001135757.1:p.Arg118del
NM_033022.3:c.352_354del	NP_148982.1:p.Arg118del
XM_011540034.1:c.505_507del	XP_011538336.1:p.Arg169del
XM_011540035.1:c.505_507del	XP_011538337.1:p.Arg169del
XM_011540036.1:c.505_507del	XP_011538338.1:p.Arg169del
XM_011540037.1:c.505_507del	XP_011538339.1:p.Arg169del
XM_011540038.1:c.505_507del	XP_011538340.1:p.Arg169del
NM_001142285.2:c.352_354del	NP_001135757.1:p.Arg118del
NM_033022.4:c.352_354del MANE Select	NP_148982.1:p.Arg118del
NM_001026.5:c.352_354del	NP_001017.1:p.Arg118del
NM_001142282.2:c.352_354del	NP_001135754.1:p.Arg118del
NM_001142283.2:c.352_354del	NP_001135755.1:p.Arg118del
NM_001142284.2:c.352_354del	NP_001135756.1:p.Arg118del