Canonical Allele Identifier: CA380140583

Gene: RAG2 RAG1

Linked Data

• MyVariant Identifiers: chr11:g.36614380A>T (hg19) ; chr11:g.36592830A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36592830A>T , CM000673.2:g.36592830A>T	GRCh38
NC_000011.9:g.36614380A>T , CM000673.1:g.36614380A>T	GRCh37
NC_000011.8:g.36570956A>T	NCBI36
NG_007573.1:g.10407T>A , LRG_99:g.10407T>A
NG_033154.1:g.3338A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000527033.6:c.1339T>A (RAG2)	ENSP00000436895.2:p.Ser447Thr
ENST00000529083.2:c.1339T>A (RAG2)	ENSP00000436327.2:p.Ser447Thr
ENST00000532616.2:c.1339T>A (RAG2)	ENSP00000432174.2:p.Ser447Thr
ENST00000311485.8:c.1339T>A (RAG2) MANE Select	ENSP00000308620.4:p.Ser447Thr
ENST00000311485.7:c.1339T>A (RAG2)	ENSP00000308620.3:p.Ser447Thr
ENST00000524423.1:n.131+5272T>A (RAG2)
ENST00000534663.1:c.*86-137A>T (RAG1)	ENSP00000434610.1:n.*86-137A>T
ENST00000618712.4:c.1339T>A (RAG2)	ENSP00000478672.1:p.Ser447Thr
NM_000536.3:c.1339T>A (RAG2)	NP_000527.2:p.Ser447Thr
NM_001243785.1:c.1339T>A (RAG2)	NP_001230714.1:p.Ser447Thr
NM_001243786.1:c.1339T>A (RAG2)	NP_001230715.1:p.Ser447Thr
NM_000536.4:c.1339T>A (RAG2) MANE Select	NP_000527.2:p.Ser447Thr
NM_001243785.2:c.1339T>A (RAG2)	NP_001230714.1:p.Ser447Thr
NM_001243786.2:c.1339T>A (RAG2)	NP_001230715.1:p.Ser447Thr