Canonical Allele Identifier: CA5571876
Gene: RPS24 HGNC NCBI

Linked Data

dbSNP Id: rs776763274

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78033900del , CM000672.2:g.78033900del GRCh38
NC_000010.10:g.79793658del , CM000672.1:g.79793658del GRCh37
NC_000010.9:g.79463664del NCBI36
NG_012633.1:g.5141del
NG_029648.1:g.641del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360830.9:c.-2del ENSP00000354074.5:n.-2del
ENST00000372360.9:c.-2del MANE Select ENSP00000361435.4:n.-2del
ENST00000440692.6:c.-2del ENSP00000414321.1:n.-2del
ENST00000464716.6:c.-2del ENSP00000494231.1:n.-2del
ENST00000465692.2:n.10del
ENST00000466129.6:n.15del
ENST00000476545.6:c.-2del ENSP00000494169.1:n.-2del
ENST00000478655.6:n.38del
ENST00000485708.7:n.38del
ENST00000613865.5:c.-2del ENSP00000478869.2:n.-2del
ENST00000645440.1:c.-2del ENSP00000496738.1:n.-2del
ENST00000645698.1:n.27del
ENST00000360830.8:c.-2del ENSP00000354074.4:n.-2del
ENST00000372360.7:c.-2del ENSP00000361435.3:n.-2del
ENST00000435275.5:c.-2del ENSP00000415549.1:n.-2del
ENST00000440692.5:c.-2del ENSP00000414321.1:n.-2del
ENST00000464716.5:n.27del
ENST00000466129.5:n.15del
ENST00000476545.5:n.23del
ENST00000478655.5:n.38del
ENST00000485708.6:n.57del
ENST00000613865.4:c.-2del ENSP00000478869.1:n.-2del
NM_001026.4:c.-2del NP_001017.1:n.-2del
NM_001142282.1:c.-2del NP_001135754.1:n.-2del
NM_001142283.1:c.-2del NP_001135755.1:n.-2del
NM_001142284.1:c.-2del NP_001135756.1:n.-2del
NM_001142285.1:c.-2del NP_001135757.1:n.-2del
NM_033022.3:c.-2del NP_148982.1:n.-2del
NM_001142285.2:c.-2del NP_001135757.1:n.-2del
NM_033022.4:c.-2del MANE Select NP_148982.1:n.-2del
NM_001026.5:c.-2del NP_001017.1:n.-2del
NM_001142282.2:c.-2del NP_001135754.1:n.-2del
NM_001142283.2:c.-2del NP_001135755.1:n.-2del
NM_001142284.2:c.-2del NP_001135756.1:n.-2del