Canonical Allele Identifier: CA2571822604

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78037285_78037291del , CM000672.2:g.78037285_78037291del	GRCh38
NC_000010.10:g.79797043_79797049del , CM000672.1:g.79797043_79797049del	GRCh37
NC_000010.9:g.79467049_79467055del	NCBI36
NG_012633.1:g.8526_8532del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.371_377del	ENSP00000354074.5:p.Asn124MetfsTer17
ENST00000372360.9:c.371_377del MANE Select	ENSP00000361435.4:p.Asn124MetfsTer16
ENST00000440692.6:c.371_377del	ENSP00000414321.1:p.Asn124MetfsTer6
ENST00000464716.6:c.371_377del	ENSP00000494231.1:p.Asn124MetfsTer23
ENST00000465692.2:n.382_388del
ENST00000476545.6:c.371_377del	ENSP00000494169.1:p.Asn124MetfsTer?
ENST00000478655.6:n.410_416del
ENST00000485708.7:n.410_416del
ENST00000613865.5:c.371_377del	ENSP00000478869.2:p.Asn124MetfsTer27
ENST00000645195.1:c.247_253del
ENST00000645440.1:c.371_377del	ENSP00000496738.1:p.Asn124MetfsTer22
ENST00000645698.1:n.399_405del
ENST00000360830.8:c.371_377del	ENSP00000354074.4:p.Asn124MetfsTer16
ENST00000372360.7:c.371_377del	ENSP00000361435.3:p.Asn124MetfsTer27
ENST00000435275.5:c.371_377del	ENSP00000415549.1:p.Asn124MetfsTer17
ENST00000440692.5:c.371_377del	ENSP00000414321.1:p.Asn124MetfsTer6
ENST00000464716.5:n.399_405del
ENST00000465692.1:n.368_374del
ENST00000476545.5:n.395_401del
ENST00000478655.5:n.410_416del
ENST00000482069.5:n.438_444del
ENST00000485708.6:n.429_435del
ENST00000613865.4:c.371_377del	ENSP00000478869.1:p.Asn124MetfsTer?
NM_001026.4:c.371_377del	NP_001017.1:p.Asn124MetfsTer27
NM_001142282.1:c.371_377del	NP_001135754.1:p.Asn124MetfsTer17
NM_001142283.1:c.371_377del	NP_001135755.1:p.Asn124MetfsTer23
NM_001142284.1:c.371_377del	NP_001135756.1:p.Asn124MetfsTer22
NM_001142285.1:c.371_377del	NP_001135757.1:p.Asn124MetfsTer6
NM_033022.3:c.371_377del	NP_148982.1:p.Asn124MetfsTer16
XM_011540034.1:c.524_530del	XP_011538336.1:p.Asn175MetfsTer27
XM_011540035.1:c.524_530del	XP_011538337.1:p.Asn175MetfsTer23
XM_011540036.1:c.524_530del	XP_011538338.1:p.Asn175MetfsTer17
XM_011540037.1:c.524_530del	XP_011538339.1:p.Asn175MetfsTer22
XM_011540038.1:c.524_530del	XP_011538340.1:p.Asn175MetfsTer16
NM_001142285.2:c.371_377del	NP_001135757.1:p.Asn124MetfsTer6
NM_033022.4:c.371_377del MANE Select	NP_148982.1:p.Asn124MetfsTer16
NM_001026.5:c.371_377del	NP_001017.1:p.Asn124MetfsTer27
NM_001142282.2:c.371_377del	NP_001135754.1:p.Asn124MetfsTer17
NM_001142283.2:c.371_377del	NP_001135755.1:p.Asn124MetfsTer23
NM_001142284.2:c.371_377del	NP_001135756.1:p.Asn124MetfsTer22