Canonical Allele Identifier: CA594423194

Gene: RPS24

Linked Data

• dbSNP Id: rs375107543
• gnomAD v2: 10-79793617-G-A
• gnomAD v4: 10-78033859-G-A
• MyVariant Identifiers: chr10:g.79793617G>A (hg19) ; chr10:g.78033859G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033859G>A , CM000672.2:g.78033859G>A	GRCh38
NC_000010.10:g.79793617G>A , CM000672.1:g.79793617G>A	GRCh37
NC_000010.9:g.79463623G>A	NCBI36
NG_012633.1:g.5100G>A
NG_029648.1:g.682C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-43G>A	ENSP00000478869.2:n.-43G>A
ENST00000645440.1:c.-43G>A	ENSP00000496738.1:n.-43G>A
ENST00000435275.5:c.-43G>A	ENSP00000415549.1:n.-43G>A
ENST00000440692.5:c.-43G>A	ENSP00000414321.1:n.-43G>A
ENST00000485708.6:n.16G>A
ENST00000613865.4:c.-43G>A	ENSP00000478869.1:n.-43G>A
NM_001026.4:c.-43G>A	NP_001017.1:n.-43G>A
NM_001142282.1:c.-43G>A	NP_001135754.1:n.-43G>A
NM_001142283.1:c.-43G>A	NP_001135755.1:n.-43G>A
NM_001142284.1:c.-43G>A	NP_001135756.1:n.-43G>A
NM_001142285.1:c.-43G>A	NP_001135757.1:n.-43G>A
NM_033022.3:c.-43G>A	NP_148982.1:n.-43G>A