Canonical Allele Identifier: CA210192401

Gene: RPS24

Linked Data

• dbSNP Id: rs918911734
• MyVariant Identifiers: chr10:g.79797103T>G (hg19) ; chr10:g.78037345T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037345T>G , CM000672.2:g.78037345T>G	GRCh38
NC_000010.10:g.79797103T>G , CM000672.1:g.79797103T>G	GRCh37
NC_000010.9:g.79467109T>G	NCBI36
NG_012633.1:g.8586T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.390+41T>G	ENSP00000354074.5:n.390+41T>G
ENST00000372360.9:c.390+41T>G MANE Select	ENSP00000361435.4:n.390+41T>G
ENST00000440692.6:c.390+41T>G	ENSP00000414321.1:n.390+41T>G
ENST00000464716.6:c.390+41T>G	ENSP00000494231.1:n.390+41T>G
ENST00000465692.2:n.401+41T>G
ENST00000476545.6:c.390+41T>G	ENSP00000494169.1:n.390+41T>G
ENST00000478655.6:n.470T>G
ENST00000485708.7:n.429+41T>G
ENST00000613865.5:c.390+41T>G	ENSP00000478869.2:n.390+41T>G
ENST00000645195.1:c.266+41T>G
ENST00000645440.1:c.390+41T>G	ENSP00000496738.1:n.390+41T>G
ENST00000645698.1:n.418+41T>G
ENST00000360830.8:c.390+41T>G	ENSP00000354074.4:n.390+41T>G
ENST00000372360.7:c.390+41T>G	ENSP00000361435.3:n.390+41T>G
ENST00000435275.5:c.390+41T>G	ENSP00000415549.1:n.390+41T>G
ENST00000440692.5:c.390+41T>G	ENSP00000414321.1:n.390+41T>G
ENST00000464716.5:n.418+41T>G
ENST00000465692.1:n.387+41T>G
ENST00000476545.5:n.414+41T>G
ENST00000478655.5:n.470T>G
ENST00000482069.5:n.457+41T>G
ENST00000485708.6:n.448+41T>G
NM_001026.4:c.390+41T>G	NP_001017.1:n.390+41T>G
NM_001142282.1:c.390+41T>G	NP_001135754.1:n.390+41T>G
NM_001142283.1:c.390+41T>G	NP_001135755.1:n.390+41T>G
NM_001142284.1:c.390+41T>G	NP_001135756.1:n.390+41T>G
NM_001142285.1:c.390+41T>G	NP_001135757.1:n.390+41T>G
NM_033022.3:c.390+41T>G	NP_148982.1:n.390+41T>G
XM_011540034.1:c.543+41T>G	XP_011538336.1:n.543+41T>G
XM_011540035.1:c.543+41T>G	XP_011538337.1:n.543+41T>G
XM_011540036.1:c.543+41T>G	XP_011538338.1:n.543+41T>G
XM_011540037.1:c.543+41T>G	XP_011538339.1:n.543+41T>G
XM_011540038.1:c.543+41T>G	XP_011538340.1:n.543+41T>G
NM_001142285.2:c.390+41T>G	NP_001135757.1:n.390+41T>G
NM_033022.4:c.390+41T>G MANE Select	NP_148982.1:n.390+41T>G
NM_001026.5:c.390+41T>G	NP_001017.1:n.390+41T>G
NM_001142282.2:c.390+41T>G	NP_001135754.1:n.390+41T>G
NM_001142283.2:c.390+41T>G	NP_001135755.1:n.390+41T>G
NM_001142284.2:c.390+41T>G	NP_001135756.1:n.390+41T>G