Canonical Allele Identifier: CA2588888012
Gene: RPS24 HGNC NCBI

Linked Data

dbSNP Id: rs2131972578

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78033800dup , CM000672.2:g.78033800dup GRCh38
NC_000010.10:g.79793558dup , CM000672.1:g.79793558dup GRCh37
NC_000010.9:g.79463564dup NCBI36
NG_012633.1:g.5041dup
NG_029648.1:g.745dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000613865.5:c.-102dup ENSP00000478869.2:n.-102dup
ENST00000435275.5:c.-102dup ENSP00000415549.1:n.-102dup
ENST00000440692.5:c.-102dup ENSP00000414321.1:n.-102dup
ENST00000613865.4:c.-102dup ENSP00000478869.1:n.-102dup
NM_001026.4:c.-102dup NP_001017.1:n.-102dup
NM_001142282.1:c.-102dup NP_001135754.1:n.-102dup
NM_001142283.1:c.-102dup NP_001135755.1:n.-102dup
NM_001142284.1:c.-102dup NP_001135756.1:n.-102dup
NM_001142285.1:c.-102dup NP_001135757.1:n.-102dup
NM_033022.3:c.-102dup NP_148982.1:n.-102dup