Canonical Allele Identifier: CA913492317

Gene: RPS24

Linked Data

• dbSNP Id: rs1564629083
• gnomAD v2: 10-79796802-CCAGCAAAAA-C
• gnomAD v3: 10-78037044-CCAGCAAAAA-C
• gnomAD v4: 10-78037044-CCAGCAAAAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037047_78037055del , CM000672.2:g.78037047_78037055del	GRCh38
NC_000010.10:g.79796805_79796813del , CM000672.1:g.79796805_79796813del	GRCh37
NC_000010.9:g.79466811_79466819del	NCBI36
NG_012633.1:g.8288_8296del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.280-147_280-139del	ENSP00000354074.5:n.280-147_280-139del
ENST00000372360.9:c.280-147_280-139del MANE Select	ENSP00000361435.4:n.280-147_280-139del
ENST00000440692.6:c.280-147_280-139del	ENSP00000414321.1:n.280-147_280-139del
ENST00000464716.6:c.280-147_280-139del	ENSP00000494231.1:n.280-147_280-139del
ENST00000465692.2:n.291-147_291-139del
ENST00000475468.6:n.690-147_690-139del
ENST00000476545.6:c.280-147_280-139del	ENSP00000494169.1:n.280-147_280-139del
ENST00000478655.6:n.319-147_319-139del
ENST00000485708.7:n.319-147_319-139del
ENST00000613865.5:c.280-147_280-139del	ENSP00000478869.2:n.280-147_280-139del
ENST00000645195.1:c.156-147_156-139del
ENST00000645440.1:c.280-147_280-139del	ENSP00000496738.1:n.280-147_280-139del
ENST00000645698.1:n.308-147_308-139del
ENST00000360830.8:c.280-147_280-139del	ENSP00000354074.4:n.280-147_280-139del
ENST00000372360.7:c.280-147_280-139del	ENSP00000361435.3:n.280-147_280-139del
ENST00000435275.5:c.280-147_280-139del	ENSP00000415549.1:n.280-147_280-139del
ENST00000440692.5:c.280-147_280-139del	ENSP00000414321.1:n.280-147_280-139del
ENST00000464716.5:n.308-147_308-139del
ENST00000465692.1:n.277-147_277-139del
ENST00000476545.5:n.304-147_304-139del
ENST00000478655.5:n.319-147_319-139del
ENST00000482069.5:n.347-147_347-139del
ENST00000485708.6:n.338-147_338-139del
ENST00000613865.4:c.280-147_280-139del	ENSP00000478869.1:n.280-147_280-139del
NM_001026.4:c.280-147_280-139del	NP_001017.1:n.280-147_280-139del
NM_001142282.1:c.280-147_280-139del	NP_001135754.1:n.280-147_280-139del
NM_001142283.1:c.280-147_280-139del	NP_001135755.1:n.280-147_280-139del
NM_001142284.1:c.280-147_280-139del	NP_001135756.1:n.280-147_280-139del
NM_001142285.1:c.280-147_280-139del	NP_001135757.1:n.280-147_280-139del
NM_033022.3:c.280-147_280-139del	NP_148982.1:n.280-147_280-139del
XM_011540034.1:c.433-147_433-139del	XP_011538336.1:n.433-147_433-139del
XM_011540035.1:c.433-147_433-139del	XP_011538337.1:n.433-147_433-139del
XM_011540036.1:c.433-147_433-139del	XP_011538338.1:n.433-147_433-139del
XM_011540037.1:c.433-147_433-139del	XP_011538339.1:n.433-147_433-139del
XM_011540038.1:c.433-147_433-139del	XP_011538340.1:n.433-147_433-139del
NM_001142285.2:c.280-147_280-139del	NP_001135757.1:n.280-147_280-139del
NM_033022.4:c.280-147_280-139del MANE Select	NP_148982.1:n.280-147_280-139del
NM_001026.5:c.280-147_280-139del	NP_001017.1:n.280-147_280-139del
NM_001142282.2:c.280-147_280-139del	NP_001135754.1:n.280-147_280-139del
NM_001142283.2:c.280-147_280-139del	NP_001135755.1:n.280-147_280-139del
NM_001142284.2:c.280-147_280-139del	NP_001135756.1:n.280-147_280-139del