Canonical Allele Identifier: CA210190854

Gene: RPS24

Linked Data

• dbSNP Id: rs533079631
• gnomAD v2: 10-79793937-GGGTAGGGGGCGGGCGGGATAGAT-G
• gnomAD v3: 10-78034179-GGGTAGGGGGCGGGCGGGATAGAT-G
• gnomAD v4: 10-78034179-GGGTAGGGGGCGGGCGGGATAGAT-G
• MyVariant Identifiers: chr10:g.79793938_79793960del (hg19) ; chr10:g.78034180_78034202del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.78034182_78034204del , CM000672.2:g.78034182_78034204del	GRCh38
NC_000010.10:g.79793940_79793962del , CM000672.1:g.79793940_79793962del	GRCh37
NC_000010.9:g.79463946_79463968del	NCBI36
NG_012633.1:g.5423_5445del
NG_029648.1:g.339_361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360830.9:c.3+278_3+300del	ENSP00000354074.5:n.3+278_3+300del
ENST00000372360.9:c.3+278_3+300del MANE Select	ENSP00000361435.4:n.3+278_3+300del
ENST00000440692.6:c.3+278_3+300del	ENSP00000414321.1:n.3+278_3+300del
ENST00000464716.6:c.3+278_3+300del	ENSP00000494231.1:n.3+278_3+300del
ENST00000465692.2:n.14+278_14+300del
ENST00000466129.6:n.19+278_19+300del
ENST00000475468.6:n.279_301del
ENST00000476545.6:c.3+278_3+300del	ENSP00000494169.1:n.3+278_3+300del
ENST00000478655.6:n.42+278_42+300del
ENST00000485708.7:n.42+278_42+300del
ENST00000613865.5:c.3+278_3+300del	ENSP00000478869.2:n.3+278_3+300del
ENST00000645440.1:c.3+278_3+300del	ENSP00000496738.1:n.3+278_3+300del
ENST00000645698.1:n.31+278_31+300del
ENST00000360830.8:c.3+278_3+300del	ENSP00000354074.4:n.3+278_3+300del
ENST00000372360.7:c.3+278_3+300del	ENSP00000361435.3:n.3+278_3+300del
ENST00000435275.5:c.3+278_3+300del	ENSP00000415549.1:n.3+278_3+300del
ENST00000440692.5:c.3+278_3+300del	ENSP00000414321.1:n.3+278_3+300del
ENST00000464716.5:n.31+278_31+300del
ENST00000466129.5:n.19+278_19+300del
ENST00000475468.5:n.279_301del
ENST00000476545.5:n.27+278_27+300del
ENST00000478655.5:n.42+278_42+300del
ENST00000482069.5:n.70+196_70+218del
ENST00000485708.6:n.61+278_61+300del
ENST00000613865.4:c.3+278_3+300del	ENSP00000478869.1:n.3+278_3+300del
NM_001026.4:c.3+278_3+300del	NP_001017.1:n.3+278_3+300del
NM_001142282.1:c.3+278_3+300del	NP_001135754.1:n.3+278_3+300del
NM_001142283.1:c.3+278_3+300del	NP_001135755.1:n.3+278_3+300del
NM_001142284.1:c.3+278_3+300del	NP_001135756.1:n.3+278_3+300del
NM_001142285.1:c.3+278_3+300del	NP_001135757.1:n.3+278_3+300del
NM_033022.3:c.3+278_3+300del	NP_148982.1:n.3+278_3+300del
NM_001142285.2:c.3+278_3+300del	NP_001135757.1:n.3+278_3+300del
NM_033022.4:c.3+278_3+300del MANE Select	NP_148982.1:n.3+278_3+300del
NM_001026.5:c.3+278_3+300del	NP_001017.1:n.3+278_3+300del
NM_001142282.2:c.3+278_3+300del	NP_001135754.1:n.3+278_3+300del
NM_001142283.2:c.3+278_3+300del	NP_001135755.1:n.3+278_3+300del
NM_001142284.2:c.3+278_3+300del	NP_001135756.1:n.3+278_3+300del