Canonical Allele Identifier: CA380140611

Gene: RAG2 RAG1

Linked Data

• ClinVar Variation Id: 1067851
• ClinVar RCV Id: RCV001379226
• dbSNP Id: rs1406618487
• gnomAD v2: 11-36614391-A-G
• gnomAD v4: 11-36592841-A-G
• MyVariant Identifiers: chr11:g.36614391A>G (hg19) ; chr11:g.36592841A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36592841A>G , CM000673.2:g.36592841A>G	GRCh38
NC_000011.9:g.36614391A>G , CM000673.1:g.36614391A>G	GRCh37
NC_000011.8:g.36570967A>G	NCBI36
NG_007573.1:g.10396T>C , LRG_99:g.10396T>C
NG_033154.1:g.3349A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.1328T>C (RAG2)	ENSP00000436895.2:p.Met443Thr
ENST00000529083.2:c.1328T>C (RAG2)	ENSP00000436327.2:p.Met443Thr
ENST00000532616.2:c.1328T>C (RAG2)	ENSP00000432174.2:p.Met443Thr
ENST00000311485.8:c.1328T>C (RAG2) MANE Select	ENSP00000308620.4:p.Met443Thr
ENST00000311485.7:c.1328T>C (RAG2)	ENSP00000308620.3:p.Met443Thr
ENST00000524423.1:n.131+5261T>C (RAG2)
ENST00000534663.1:c.*86-126A>G (RAG1)	ENSP00000434610.1:n.*86-126A>G
ENST00000618712.4:c.1328T>C (RAG2)	ENSP00000478672.1:p.Met443Thr
NM_000536.3:c.1328T>C (RAG2)	NP_000527.2:p.Met443Thr
NM_001243785.1:c.1328T>C (RAG2)	NP_001230714.1:p.Met443Thr
NM_001243786.1:c.1328T>C (RAG2)	NP_001230715.1:p.Met443Thr
NM_000536.4:c.1328T>C (RAG2) MANE Select	NP_000527.2:p.Met443Thr
NM_001243785.2:c.1328T>C (RAG2)	NP_001230714.1:p.Met443Thr
NM_001243786.2:c.1328T>C (RAG2)	NP_001230715.1:p.Met443Thr