Canonical Allele Identifier: CA2609827945

Gene: RPS24

Linked Data

• gnomAD v4: 10-78035238-CGCTACATGACTAATGGCTA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78035239_78035257del , CM000672.2:g.78035239_78035257del	GRCh38
NC_000010.10:g.79794997_79795015del , CM000672.1:g.79794997_79795015del	GRCh37
NC_000010.9:g.79465003_79465021del	NCBI36
NG_012633.1:g.6480_6498del

Transcript Alleles

HGVS	Amino-acid change
ENST00000360830.9:c.4-113_4-95del	ENSP00000354074.5:n.4-113_4-95del
ENST00000372360.9:c.4-113_4-95del MANE Select	ENSP00000361435.4:n.4-113_4-95del
ENST00000440692.6:c.4-113_4-95del	ENSP00000414321.1:n.4-113_4-95del
ENST00000464716.6:c.4-113_4-95del	ENSP00000494231.1:n.4-113_4-95del
ENST00000465692.2:n.15-113_15-95del
ENST00000466129.6:n.20-113_20-95del
ENST00000475468.6:n.414-113_414-95del
ENST00000476545.6:c.4-113_4-95del	ENSP00000494169.1:n.4-113_4-95del
ENST00000478655.6:n.43-113_43-95del
ENST00000485708.7:n.43-113_43-95del
ENST00000613865.5:c.4-113_4-95del	ENSP00000478869.2:n.4-113_4-95del
ENST00000645440.1:c.4-113_4-95del	ENSP00000496738.1:n.4-113_4-95del
ENST00000645698.1:n.32-113_32-95del
ENST00000646254.1:n.213-113_213-95del
ENST00000360830.8:c.4-113_4-95del	ENSP00000354074.4:n.4-113_4-95del
ENST00000372360.7:c.4-113_4-95del	ENSP00000361435.3:n.4-113_4-95del
ENST00000435275.5:c.4-113_4-95del	ENSP00000415549.1:n.4-113_4-95del
ENST00000440692.5:c.4-113_4-95del	ENSP00000414321.1:n.4-113_4-95del
ENST00000464716.5:n.32-113_32-95del
ENST00000466129.5:n.20-113_20-95del
ENST00000475468.5:n.414-113_414-95del
ENST00000476545.5:n.28-113_28-95del
ENST00000478655.5:n.43-113_43-95del
ENST00000482069.5:n.71-113_71-95del
ENST00000485708.6:n.62-113_62-95del
ENST00000613865.4:c.4-113_4-95del	ENSP00000478869.1:n.4-113_4-95del
NM_001026.4:c.4-113_4-95del	NP_001017.1:n.4-113_4-95del
NM_001142282.1:c.4-113_4-95del	NP_001135754.1:n.4-113_4-95del
NM_001142283.1:c.4-113_4-95del	NP_001135755.1:n.4-113_4-95del
NM_001142284.1:c.4-113_4-95del	NP_001135756.1:n.4-113_4-95del
NM_001142285.1:c.4-113_4-95del	NP_001135757.1:n.4-113_4-95del
NM_033022.3:c.4-113_4-95del	NP_148982.1:n.4-113_4-95del
XM_011540034.1:c.157-113_157-95del	XP_011538336.1:n.157-113_157-95del
XM_011540035.1:c.157-113_157-95del	XP_011538337.1:n.157-113_157-95del
XM_011540036.1:c.157-113_157-95del	XP_011538338.1:n.157-113_157-95del
XM_011540037.1:c.157-113_157-95del	XP_011538339.1:n.157-113_157-95del
XM_011540038.1:c.157-113_157-95del	XP_011538340.1:n.157-113_157-95del
NM_001142285.2:c.4-113_4-95del	NP_001135757.1:n.4-113_4-95del
NM_033022.4:c.4-113_4-95del MANE Select	NP_148982.1:n.4-113_4-95del
NM_001026.5:c.4-113_4-95del	NP_001017.1:n.4-113_4-95del
NM_001142282.2:c.4-113_4-95del	NP_001135754.1:n.4-113_4-95del
NM_001142283.2:c.4-113_4-95del	NP_001135755.1:n.4-113_4-95del
NM_001142284.2:c.4-113_4-95del	NP_001135756.1:n.4-113_4-95del