Canonical Allele Identifier: CA2613151060

Gene: RAG2

Linked Data

• gnomAD v4: 11-36593976-C-CAAACACTTTATAGGTTATTTGTTACCAAGACTTATATAATAAATATAAACATACCT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36593976_36593977insAAACACTTTATAGGTTATTTGTTACCAAGACTTATATAATAAATATAAACATACCT , CM000673.2:g.36593976_36593977insAAACACTTTATAGGTTATTTGTTACCAAGACTTATATAATAAATATAAACATACCT	GRCh38
NC_000011.9:g.36615526_36615527insAAACACTTTATAGGTTATTTGTTACCAAGACTTATATAATAAATATAAACATACCT , CM000673.1:g.36615526_36615527insAAACACTTTATAGGTTATTTGTTACCAAGACTTATATAATAAATATAAACATACCT	GRCh37
NC_000011.8:g.36572102_36572103insAAACACTTTATAGGTTATTTGTTACCAAGACTTATATAATAAATATAAACATACCT	NCBI36
NG_007573.1:g.9260_9261insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT , LRG_99:g.9260_9261insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT
NG_033154.1:g.4484_4485insAAACACTTTATAGGTTATTTGTTACCAAGACTTATATAATAAATATAAACATACCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	ENSP00000436895.2:p.Asp65ArgfsTer14
ENST00000529083.2:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	ENSP00000436327.2:p.Asp65ArgfsTer14
ENST00000532616.2:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	ENSP00000432174.2:p.Asp65ArgfsTer14
ENST00000311485.8:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT MANE Select	ENSP00000308620.4:p.Asp65ArgfsTer14
ENST00000311485.7:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	ENSP00000308620.3:p.Asp65ArgfsTer14
ENST00000524423.1:n.131+4125_131+4126insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT
ENST00000527033.5:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	ENSP00000436895.1:p.Asp65ArgfsTer14
ENST00000529083.1:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	ENSP00000436327.1:p.Asp65ArgfsTer14
ENST00000618712.4:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	ENSP00000478672.1:p.Asp65ArgfsTer14
NM_000536.3:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	NP_000527.2:p.Asp65ArgfsTer14
NM_001243785.1:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	NP_001230714.1:p.Asp65ArgfsTer14
NM_001243786.1:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	NP_001230715.1:p.Asp65ArgfsTer14
NM_000536.4:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT MANE Select	NP_000527.2:p.Asp65ArgfsTer14
NM_001243785.2:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	NP_001230714.1:p.Asp65ArgfsTer14
NM_001243786.2:c.192_193insAGGTATGTTTATATTTATTATATAAGTCTTGGTAACAAATAACCTATAAAGTGTTT	NP_001230715.1:p.Asp65ArgfsTer14