Canonical Allele Identifier: CA377326425

Gene: RPS24

Linked Data

• ClinVar Variation Id: 1698829
• ClinVar RCV Id: RCV002272686
• dbSNP Id: rs2131972918
• MyVariant Identifiers: chr10:g.79793662G>A (hg19) ; chr10:g.78033904G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033904G>A , CM000672.2:g.78033904G>A	GRCh38
NC_000010.10:g.79793662G>A , CM000672.1:g.79793662G>A	GRCh37
NC_000010.9:g.79463668G>A	NCBI36
NG_012633.1:g.5145G>A
NG_029648.1:g.637C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.3G>A	ENSP00000354074.5:p.Met1Ile
ENST00000372360.9:c.3G>A MANE Select	ENSP00000361435.4:p.Met1Ile
ENST00000440692.6:c.3G>A	ENSP00000414321.1:p.Met1Ile
ENST00000464716.6:c.3G>A	ENSP00000494231.1:p.Met1Ile
ENST00000465692.2:n.14G>A
ENST00000466129.6:n.19G>A
ENST00000475468.6:n.1G>A
ENST00000476545.6:c.3G>A	ENSP00000494169.1:p.Met1Ile
ENST00000478655.6:n.42G>A
ENST00000485708.7:n.42G>A
ENST00000613865.5:c.3G>A	ENSP00000478869.2:p.Met1Ile
ENST00000645440.1:c.3G>A	ENSP00000496738.1:p.Met1Ile
ENST00000645698.1:n.31G>A
ENST00000360830.8:c.3G>A	ENSP00000354074.4:p.Met1Ile
ENST00000372360.7:c.3G>A	ENSP00000361435.3:p.Met1Ile
ENST00000435275.5:c.3G>A	ENSP00000415549.1:p.Met1Ile
ENST00000440692.5:c.3G>A	ENSP00000414321.1:p.Met1Ile
ENST00000464716.5:n.31G>A
ENST00000466129.5:n.19G>A
ENST00000475468.5:n.1G>A
ENST00000476545.5:n.27G>A
ENST00000478655.5:n.42G>A
ENST00000485708.6:n.61G>A
ENST00000613865.4:c.3G>A	ENSP00000478869.1:p.Met1Ile
NM_001026.4:c.3G>A	NP_001017.1:p.Met1Ile
NM_001142282.1:c.3G>A	NP_001135754.1:p.Met1Ile
NM_001142283.1:c.3G>A	NP_001135755.1:p.Met1Ile
NM_001142284.1:c.3G>A	NP_001135756.1:p.Met1Ile
NM_001142285.1:c.3G>A	NP_001135757.1:p.Met1Ile
NM_033022.3:c.3G>A	NP_148982.1:p.Met1Ile
NM_001142285.2:c.3G>A	NP_001135757.1:p.Met1Ile
NM_033022.4:c.3G>A MANE Select	NP_148982.1:p.Met1Ile
NM_001026.5:c.3G>A	NP_001017.1:p.Met1Ile
NM_001142282.2:c.3G>A	NP_001135754.1:p.Met1Ile
NM_001142283.2:c.3G>A	NP_001135755.1:p.Met1Ile
NM_001142284.2:c.3G>A	NP_001135756.1:p.Met1Ile