Canonical Allele Identifier: CA2609826143

Gene: RPS24

Linked Data

• gnomAD v4: 10-78033839-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78033839A>C , CM000672.2:g.78033839A>C	GRCh38
NC_000010.10:g.79793597A>C , CM000672.1:g.79793597A>C	GRCh37
NC_000010.9:g.79463603A>C	NCBI36
NG_012633.1:g.5080A>C
NG_029648.1:g.702T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000613865.5:c.-63A>C	ENSP00000478869.2:n.-63A>C
ENST00000645440.1:c.-63A>C	ENSP00000496738.1:n.-63A>C
ENST00000435275.5:c.-63A>C	ENSP00000415549.1:n.-63A>C
ENST00000440692.5:c.-63A>C	ENSP00000414321.1:n.-63A>C
ENST00000613865.4:c.-63A>C	ENSP00000478869.1:n.-63A>C
NM_001026.4:c.-63A>C	NP_001017.1:n.-63A>C
NM_001142282.1:c.-63A>C	NP_001135754.1:n.-63A>C
NM_001142283.1:c.-63A>C	NP_001135755.1:n.-63A>C
NM_001142284.1:c.-63A>C	NP_001135756.1:n.-63A>C
NM_001142285.1:c.-63A>C	NP_001135757.1:n.-63A>C
NM_033022.3:c.-63A>C	NP_148982.1:n.-63A>C