Canonical Allele Identifier: CA2574592243

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037303_78037305del , CM000672.2:g.78037303_78037305del	GRCh38
NC_000010.10:g.79797061_79797063del , CM000672.1:g.79797061_79797063del	GRCh37
NC_000010.9:g.79467067_79467069del	NCBI36
NG_012633.1:g.8544_8546del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.389_390+1del
ENST00000372360.9:c.389_390+1del
ENST00000440692.6:c.389_390+1del
ENST00000464716.6:c.389_390+1del
ENST00000465692.2:n.400_401+1del
ENST00000476545.6:c.389_390+1del
ENST00000478655.6:n.428_430del
ENST00000485708.7:n.428_429+1del
ENST00000613865.5:c.389_390+1del
ENST00000645195.1:c.265_266+1del
ENST00000645440.1:c.389_390+1del
ENST00000645698.1:n.417_418+1del
ENST00000360830.8:c.389_390+1del
ENST00000372360.7:c.389_390+1del
ENST00000435275.5:c.389_390+1del
ENST00000440692.5:c.389_390+1del
ENST00000464716.5:n.417_418+1del
ENST00000465692.1:n.386_387+1del
ENST00000476545.5:n.413_414+1del
ENST00000478655.5:n.428_430del
ENST00000482069.5:n.456_457+1del
ENST00000485708.6:n.447_448+1del
ENST00000613865.4:c.389_390+1del
NM_001026.4:c.389_390+1del
NM_001142282.1:c.389_390+1del
NM_001142283.1:c.389_390+1del
NM_001142284.1:c.389_390+1del
NM_001142285.1:c.389_390+1del
NM_033022.3:c.389_390+1del
XM_011540034.1:c.542_543+1del
XM_011540035.1:c.542_543+1del
XM_011540036.1:c.542_543+1del
XM_011540037.1:c.542_543+1del
XM_011540038.1:c.542_543+1del
NM_001142285.2:c.389_390+1del
NM_033022.4:c.389_390+1del
NM_001026.5:c.389_390+1del
NM_001142282.2:c.389_390+1del
NM_001142283.2:c.389_390+1del
NM_001142284.2:c.389_390+1del