Canonical Allele Identifier: CA210192302

Gene: RPS24

Linked Data

• dbSNP Id: rs1025342367
• gnomAD v4: 10-78037273-C-T
• MyVariant Identifiers: chr10:g.79797031C>T (hg19) ; chr10:g.78037273C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037273C>T , CM000672.2:g.78037273C>T	GRCh38
NC_000010.10:g.79797031C>T , CM000672.1:g.79797031C>T	GRCh37
NC_000010.9:g.79467037C>T	NCBI36
NG_012633.1:g.8514C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.359C>T	ENSP00000354074.5:p.Thr120Ile
ENST00000372360.9:c.359C>T MANE Select	ENSP00000361435.4:p.Thr120Ile
ENST00000440692.6:c.359C>T	ENSP00000414321.1:p.Thr120Ile
ENST00000464716.6:c.359C>T	ENSP00000494231.1:p.Thr120Ile
ENST00000465692.2:n.370C>T
ENST00000476545.6:c.359C>T	ENSP00000494169.1:p.Thr120Ile
ENST00000478655.6:n.398C>T
ENST00000485708.7:n.398C>T
ENST00000613865.5:c.359C>T	ENSP00000478869.2:p.Thr120Ile
ENST00000645195.1:c.235C>T
ENST00000645440.1:c.359C>T	ENSP00000496738.1:p.Thr120Ile
ENST00000645698.1:n.387C>T
ENST00000360830.8:c.359C>T	ENSP00000354074.4:p.Thr120Ile
ENST00000372360.7:c.359C>T	ENSP00000361435.3:p.Thr120Ile
ENST00000435275.5:c.359C>T	ENSP00000415549.1:p.Thr120Ile
ENST00000440692.5:c.359C>T	ENSP00000414321.1:p.Thr120Ile
ENST00000464716.5:n.387C>T
ENST00000465692.1:n.356C>T
ENST00000476545.5:n.383C>T
ENST00000478655.5:n.398C>T
ENST00000482069.5:n.426C>T
ENST00000485708.6:n.417C>T
ENST00000613865.4:c.359C>T	ENSP00000478869.1:p.Thr120Ile
NM_001026.4:c.359C>T	NP_001017.1:p.Thr120Ile
NM_001142282.1:c.359C>T	NP_001135754.1:p.Thr120Ile
NM_001142283.1:c.359C>T	NP_001135755.1:p.Thr120Ile
NM_001142284.1:c.359C>T	NP_001135756.1:p.Thr120Ile
NM_001142285.1:c.359C>T	NP_001135757.1:p.Thr120Ile
NM_033022.3:c.359C>T	NP_148982.1:p.Thr120Ile
XM_011540034.1:c.512C>T	XP_011538336.1:p.Thr171Ile
XM_011540035.1:c.512C>T	XP_011538337.1:p.Thr171Ile
XM_011540036.1:c.512C>T	XP_011538338.1:p.Thr171Ile
XM_011540037.1:c.512C>T	XP_011538339.1:p.Thr171Ile
XM_011540038.1:c.512C>T	XP_011538340.1:p.Thr171Ile
NM_001142285.2:c.359C>T	NP_001135757.1:p.Thr120Ile
NM_033022.4:c.359C>T MANE Select	NP_148982.1:p.Thr120Ile
NM_001026.5:c.359C>T	NP_001017.1:p.Thr120Ile
NM_001142282.2:c.359C>T	NP_001135754.1:p.Thr120Ile
NM_001142283.2:c.359C>T	NP_001135755.1:p.Thr120Ile
NM_001142284.2:c.359C>T	NP_001135756.1:p.Thr120Ile