Canonical Allele Identifier: CA930215385
Gene: RPS24 HGNC NCBI

Linked Data

dbSNP Id: rs1847801029

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.78034029_78034030del , CM000672.2:g.78034029_78034030del GRCh38
NC_000010.10:g.79793787_79793788del , CM000672.1:g.79793787_79793788del GRCh37
NC_000010.9:g.79463793_79463794del NCBI36
NG_012633.1:g.5270_5271del
NG_029648.1:g.513_514del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360830.9:c.3+125_3+126del ENSP00000354074.5:n.3+125_3+126del
ENST00000372360.9:c.3+125_3+126del MANE Select ENSP00000361435.4:n.3+125_3+126del
ENST00000440692.6:c.3+125_3+126del ENSP00000414321.1:n.3+125_3+126del
ENST00000464716.6:c.3+125_3+126del ENSP00000494231.1:n.3+125_3+126del
ENST00000465692.2:n.14+125_14+126del
ENST00000466129.6:n.19+125_19+126del
ENST00000475468.6:n.126_127del
ENST00000476545.6:c.3+125_3+126del ENSP00000494169.1:n.3+125_3+126del
ENST00000478655.6:n.42+125_42+126del
ENST00000485708.7:n.42+125_42+126del
ENST00000613865.5:c.3+125_3+126del ENSP00000478869.2:n.3+125_3+126del
ENST00000645440.1:c.3+125_3+126del ENSP00000496738.1:n.3+125_3+126del
ENST00000645698.1:n.31+125_31+126del
ENST00000360830.8:c.3+125_3+126del ENSP00000354074.4:n.3+125_3+126del
ENST00000372360.7:c.3+125_3+126del ENSP00000361435.3:n.3+125_3+126del
ENST00000435275.5:c.3+125_3+126del ENSP00000415549.1:n.3+125_3+126del
ENST00000440692.5:c.3+125_3+126del ENSP00000414321.1:n.3+125_3+126del
ENST00000464716.5:n.31+125_31+126del
ENST00000466129.5:n.19+125_19+126del
ENST00000475468.5:n.126_127del
ENST00000476545.5:n.27+125_27+126del
ENST00000478655.5:n.42+125_42+126del
ENST00000482069.5:n.70+43_70+44del
ENST00000485708.6:n.61+125_61+126del
ENST00000613865.4:c.3+125_3+126del ENSP00000478869.1:n.3+125_3+126del
NM_001026.4:c.3+125_3+126del NP_001017.1:n.3+125_3+126del
NM_001142282.1:c.3+125_3+126del NP_001135754.1:n.3+125_3+126del
NM_001142283.1:c.3+125_3+126del NP_001135755.1:n.3+125_3+126del
NM_001142284.1:c.3+125_3+126del NP_001135756.1:n.3+125_3+126del
NM_001142285.1:c.3+125_3+126del NP_001135757.1:n.3+125_3+126del
NM_033022.3:c.3+125_3+126del NP_148982.1:n.3+125_3+126del
NM_001142285.2:c.3+125_3+126del NP_001135757.1:n.3+125_3+126del
NM_033022.4:c.3+125_3+126del MANE Select NP_148982.1:n.3+125_3+126del
NM_001026.5:c.3+125_3+126del NP_001017.1:n.3+125_3+126del
NM_001142282.2:c.3+125_3+126del NP_001135754.1:n.3+125_3+126del
NM_001142283.2:c.3+125_3+126del NP_001135755.1:n.3+125_3+126del
NM_001142284.2:c.3+125_3+126del NP_001135756.1:n.3+125_3+126del