Canonical Allele Identifier: CA1921522475

Gene: RPS24

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78034010_78034020delinsCTCTGGCCGTT , CM000672.2:g.78034010_78034020delinsCTCTGGCCGTT	GRCh38
NC_000010.10:g.79793768_79793778delinsCTCTGGCCGTT , CM000672.1:g.79793768_79793778delinsCTCTGGCCGTT	GRCh37
NC_000010.9:g.79463774_79463784delinsCTCTGGCCGTT	NCBI36
NG_012633.1:g.5251_5261delinsCTCTGGCCGTT
NG_029648.1:g.521_531delinsAACGGCCAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000354074.5:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000372360.9:c.3+106_3+116delinsCTCTGGCCGTT MANE Select	ENSP00000361435.4:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000440692.6:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000414321.1:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000464716.6:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000494231.1:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000465692.2:n.14+106_14+116delinsCTCTGGCCGTT
ENST00000466129.6:n.19+106_19+116delinsCTCTGGCCGTT
ENST00000475468.6:n.107_117delinsCTCTGGCCGTT
ENST00000476545.6:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000494169.1:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000478655.6:n.42+106_42+116delinsCTCTGGCCGTT
ENST00000485708.7:n.42+106_42+116delinsCTCTGGCCGTT
ENST00000613865.5:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000478869.2:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000645440.1:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000496738.1:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000645698.1:n.31+106_31+116delinsCTCTGGCCGTT
ENST00000360830.8:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000354074.4:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000372360.7:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000361435.3:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000435275.5:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000415549.1:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000440692.5:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000414321.1:n.3+106_3+116delinsCTCTGGCCGTT
ENST00000464716.5:n.31+106_31+116delinsCTCTGGCCGTT
ENST00000466129.5:n.19+106_19+116delinsCTCTGGCCGTT
ENST00000475468.5:n.107_117delinsCTCTGGCCGTT
ENST00000476545.5:n.27+106_27+116delinsCTCTGGCCGTT
ENST00000478655.5:n.42+106_42+116delinsCTCTGGCCGTT
ENST00000482069.5:n.70+24_70+34delinsCTCTGGCCGTT
ENST00000485708.6:n.61+106_61+116delinsCTCTGGCCGTT
ENST00000613865.4:c.3+106_3+116delinsCTCTGGCCGTT	ENSP00000478869.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001026.4:c.3+106_3+116delinsCTCTGGCCGTT	NP_001017.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142282.1:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135754.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142283.1:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135755.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142284.1:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135756.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142285.1:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135757.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_033022.3:c.3+106_3+116delinsCTCTGGCCGTT	NP_148982.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142285.2:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135757.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_033022.4:c.3+106_3+116delinsCTCTGGCCGTT MANE Select	NP_148982.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001026.5:c.3+106_3+116delinsCTCTGGCCGTT	NP_001017.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142282.2:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135754.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142283.2:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135755.1:n.3+106_3+116delinsCTCTGGCCGTT
NM_001142284.2:c.3+106_3+116delinsCTCTGGCCGTT	NP_001135756.1:n.3+106_3+116delinsCTCTGGCCGTT