Canonical Allele Identifier: CA5571838

Gene: RPS24

Linked Data

• dbSNP Id: rs201666642
• ExAC: 10:79793612 A / C
• gnomAD v2: 10-79793612-A-C
• gnomAD v3: 10-78033854-A-C
• gnomAD v4: 10-78033854-A-C
• MyVariant Identifiers: chr10:g.79793612A>C (hg19) ; chr10:g.78033854A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033854A>C , CM000672.2:g.78033854A>C	GRCh38
NC_000010.10:g.79793612A>C , CM000672.1:g.79793612A>C	GRCh37
NC_000010.9:g.79463618A>C	NCBI36
NG_012633.1:g.5095A>C
NG_029648.1:g.687T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-48A>C	ENSP00000478869.2:n.-48A>C
ENST00000645440.1:c.-48A>C	ENSP00000496738.1:n.-48A>C
ENST00000435275.5:c.-48A>C	ENSP00000415549.1:n.-48A>C
ENST00000440692.5:c.-48A>C	ENSP00000414321.1:n.-48A>C
ENST00000485708.6:n.11A>C
ENST00000613865.4:c.-48A>C	ENSP00000478869.1:n.-48A>C
NM_001026.4:c.-48A>C	NP_001017.1:n.-48A>C
NM_001142282.1:c.-48A>C	NP_001135754.1:n.-48A>C
NM_001142283.1:c.-48A>C	NP_001135755.1:n.-48A>C
NM_001142284.1:c.-48A>C	NP_001135756.1:n.-48A>C
NM_001142285.1:c.-48A>C	NP_001135757.1:n.-48A>C
NM_033022.3:c.-48A>C	NP_148982.1:n.-48A>C