Canonical Allele Identifier: CA210192207

Gene: RPS24

Linked Data

• dbSNP Id: rs376045832
• gnomAD v2: 10-79796784-TTGA-T
• gnomAD v3: 10-78037026-TTGA-T
• gnomAD v4: 10-78037026-TTGA-T
• MyVariant Identifiers: chr10:g.79796785_79796787del (hg19) ; chr10:g.78037027_78037029del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037031_78037033del , CM000672.2:g.78037031_78037033del	GRCh38
NC_000010.10:g.79796789_79796791del , CM000672.1:g.79796789_79796791del	GRCh37
NC_000010.9:g.79466795_79466797del	NCBI36
NG_012633.1:g.8272_8274del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.280-163_280-161del	ENSP00000354074.5:n.280-163_280-161del
ENST00000372360.9:c.280-163_280-161del MANE Select	ENSP00000361435.4:n.280-163_280-161del
ENST00000440692.6:c.280-163_280-161del	ENSP00000414321.1:n.280-163_280-161del
ENST00000464716.6:c.280-163_280-161del	ENSP00000494231.1:n.280-163_280-161del
ENST00000465692.2:n.291-163_291-161del
ENST00000475468.6:n.690-163_690-161del
ENST00000476545.6:c.280-163_280-161del	ENSP00000494169.1:n.280-163_280-161del
ENST00000478655.6:n.319-163_319-161del
ENST00000485708.7:n.319-163_319-161del
ENST00000613865.5:c.280-163_280-161del	ENSP00000478869.2:n.280-163_280-161del
ENST00000645195.1:c.156-163_156-161del
ENST00000645440.1:c.280-163_280-161del	ENSP00000496738.1:n.280-163_280-161del
ENST00000645698.1:n.308-163_308-161del
ENST00000360830.8:c.280-163_280-161del	ENSP00000354074.4:n.280-163_280-161del
ENST00000372360.7:c.280-163_280-161del	ENSP00000361435.3:n.280-163_280-161del
ENST00000435275.5:c.280-163_280-161del	ENSP00000415549.1:n.280-163_280-161del
ENST00000440692.5:c.280-163_280-161del	ENSP00000414321.1:n.280-163_280-161del
ENST00000464716.5:n.308-163_308-161del
ENST00000465692.1:n.277-163_277-161del
ENST00000476545.5:n.304-163_304-161del
ENST00000478655.5:n.319-163_319-161del
ENST00000482069.5:n.347-163_347-161del
ENST00000485708.6:n.338-163_338-161del
ENST00000613865.4:c.280-163_280-161del	ENSP00000478869.1:n.280-163_280-161del
NM_001026.4:c.280-163_280-161del	NP_001017.1:n.280-163_280-161del
NM_001142282.1:c.280-163_280-161del	NP_001135754.1:n.280-163_280-161del
NM_001142283.1:c.280-163_280-161del	NP_001135755.1:n.280-163_280-161del
NM_001142284.1:c.280-163_280-161del	NP_001135756.1:n.280-163_280-161del
NM_001142285.1:c.280-163_280-161del	NP_001135757.1:n.280-163_280-161del
NM_033022.3:c.280-163_280-161del	NP_148982.1:n.280-163_280-161del
XM_011540034.1:c.433-163_433-161del	XP_011538336.1:n.433-163_433-161del
XM_011540035.1:c.433-163_433-161del	XP_011538337.1:n.433-163_433-161del
XM_011540036.1:c.433-163_433-161del	XP_011538338.1:n.433-163_433-161del
XM_011540037.1:c.433-163_433-161del	XP_011538339.1:n.433-163_433-161del
XM_011540038.1:c.433-163_433-161del	XP_011538340.1:n.433-163_433-161del
NM_001142285.2:c.280-163_280-161del	NP_001135757.1:n.280-163_280-161del
NM_033022.4:c.280-163_280-161del MANE Select	NP_148982.1:n.280-163_280-161del
NM_001026.5:c.280-163_280-161del	NP_001017.1:n.280-163_280-161del
NM_001142282.2:c.280-163_280-161del	NP_001135754.1:n.280-163_280-161del
NM_001142283.2:c.280-163_280-161del	NP_001135755.1:n.280-163_280-161del
NM_001142284.2:c.280-163_280-161del	NP_001135756.1:n.280-163_280-161del