Canonical Allele Identifier: CA1921524111

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037093_78037095delinsCTG , CM000672.2:g.78037093_78037095delinsCTG	GRCh38
NC_000010.10:g.79796851_79796853delinsCTG , CM000672.1:g.79796851_79796853delinsCTG	GRCh37
NC_000010.9:g.79466857_79466859delinsCTG	NCBI36
NG_012633.1:g.8334_8336delinsCTG

Transcript Alleles

HGVS	Amino-acid change
ENST00000360830.9:c.280-101_280-99delinsCTG	ENSP00000354074.5:n.280-101_280-99delinsCTG
ENST00000372360.9:c.280-101_280-99delinsCTG MANE Select	ENSP00000361435.4:n.280-101_280-99delinsCTG
ENST00000440692.6:c.280-101_280-99delinsCTG	ENSP00000414321.1:n.280-101_280-99delinsCTG
ENST00000464716.6:c.280-101_280-99delinsCTG	ENSP00000494231.1:n.280-101_280-99delinsCTG
ENST00000465692.2:n.291-101_291-99delinsCTG
ENST00000475468.6:n.690-101_690-99delinsCTG
ENST00000476545.6:c.280-101_280-99delinsCTG	ENSP00000494169.1:n.280-101_280-99delinsCTG
ENST00000478655.6:n.319-101_319-99delinsCTG
ENST00000485708.7:n.319-101_319-99delinsCTG
ENST00000613865.5:c.280-101_280-99delinsCTG	ENSP00000478869.2:n.280-101_280-99delinsCTG
ENST00000645195.1:c.156-101_156-99delinsCTG
ENST00000645440.1:c.280-101_280-99delinsCTG	ENSP00000496738.1:n.280-101_280-99delinsCTG
ENST00000645698.1:n.308-101_308-99delinsCTG
ENST00000360830.8:c.280-101_280-99delinsCTG	ENSP00000354074.4:n.280-101_280-99delinsCTG
ENST00000372360.7:c.280-101_280-99delinsCTG	ENSP00000361435.3:n.280-101_280-99delinsCTG
ENST00000435275.5:c.280-101_280-99delinsCTG	ENSP00000415549.1:n.280-101_280-99delinsCTG
ENST00000440692.5:c.280-101_280-99delinsCTG	ENSP00000414321.1:n.280-101_280-99delinsCTG
ENST00000464716.5:n.308-101_308-99delinsCTG
ENST00000465692.1:n.277-101_277-99delinsCTG
ENST00000476545.5:n.304-101_304-99delinsCTG
ENST00000478655.5:n.319-101_319-99delinsCTG
ENST00000482069.5:n.347-101_347-99delinsCTG
ENST00000485708.6:n.338-101_338-99delinsCTG
ENST00000613865.4:c.280-101_280-99delinsCTG	ENSP00000478869.1:n.280-101_280-99delinsCTG
NM_001026.4:c.280-101_280-99delinsCTG	NP_001017.1:n.280-101_280-99delinsCTG
NM_001142282.1:c.280-101_280-99delinsCTG	NP_001135754.1:n.280-101_280-99delinsCTG
NM_001142283.1:c.280-101_280-99delinsCTG	NP_001135755.1:n.280-101_280-99delinsCTG
NM_001142284.1:c.280-101_280-99delinsCTG	NP_001135756.1:n.280-101_280-99delinsCTG
NM_001142285.1:c.280-101_280-99delinsCTG	NP_001135757.1:n.280-101_280-99delinsCTG
NM_033022.3:c.280-101_280-99delinsCTG	NP_148982.1:n.280-101_280-99delinsCTG
XM_011540034.1:c.433-101_433-99delinsCTG	XP_011538336.1:n.433-101_433-99delinsCTG
XM_011540035.1:c.433-101_433-99delinsCTG	XP_011538337.1:n.433-101_433-99delinsCTG
XM_011540036.1:c.433-101_433-99delinsCTG	XP_011538338.1:n.433-101_433-99delinsCTG
XM_011540037.1:c.433-101_433-99delinsCTG	XP_011538339.1:n.433-101_433-99delinsCTG
XM_011540038.1:c.433-101_433-99delinsCTG	XP_011538340.1:n.433-101_433-99delinsCTG
NM_001142285.2:c.280-101_280-99delinsCTG	NP_001135757.1:n.280-101_280-99delinsCTG
NM_033022.4:c.280-101_280-99delinsCTG MANE Select	NP_148982.1:n.280-101_280-99delinsCTG
NM_001026.5:c.280-101_280-99delinsCTG	NP_001017.1:n.280-101_280-99delinsCTG
NM_001142282.2:c.280-101_280-99delinsCTG	NP_001135754.1:n.280-101_280-99delinsCTG
NM_001142283.2:c.280-101_280-99delinsCTG	NP_001135755.1:n.280-101_280-99delinsCTG
NM_001142284.2:c.280-101_280-99delinsCTG	NP_001135756.1:n.280-101_280-99delinsCTG