Canonical Allele Identifier: CA2613151160
Gene: RAG2 HGNC NCBI
IFTAP HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36594316_36594320del , CM000673.2:g.36594316_36594320del GRCh38
NC_000011.9:g.36615866_36615870del , CM000673.1:g.36615866_36615870del GRCh37
NC_000011.8:g.36572442_36572446del NCBI36
NG_007573.1:g.8917_8921del , LRG_99:g.8917_8921del
NG_033154.1:g.4824_4828del

Transcript Alleles

HGVS Amino-acid Change
ENST00000527033.6:c.-27-125_-27-121del (RAG2) ENSP00000436895.2:n.-27-125_-27-121del
ENST00000529083.2:c.-27-125_-27-121del (RAG2) ENSP00000436327.2:n.-27-125_-27-121del
ENST00000532616.2:c.-27-125_-27-121del (RAG2) ENSP00000432174.2:n.-27-125_-27-121del
ENST00000311485.8:c.-27-125_-27-121del (RAG2) MANE Select ENSP00000308620.4:n.-27-125_-27-121del
ENST00000311485.7:c.-27-125_-27-121del (RAG2) ENSP00000308620.3:n.-27-125_-27-121del
ENST00000524423.1:n.131+3782_131+3786del (RAG2)
ENST00000527033.5:c.-27-125_-27-121del (RAG2) ENSP00000436895.1:n.-27-125_-27-121del
ENST00000529083.1:c.-27-125_-27-121del (RAG2) ENSP00000436327.1:n.-27-125_-27-121del
ENST00000532616.1:c.-27-125_-27-121del (RAG2) ENSP00000432174.1:n.-27-125_-27-121del
ENST00000618712.4:c.-27-125_-27-121del (RAG2) ENSP00000478672.1:n.-27-125_-27-121del
NM_000536.3:c.-27-125_-27-121del (RAG2) NP_000527.2:n.-27-125_-27-121del
NM_001243785.1:c.-27-125_-27-121del (RAG2) NP_001230714.1:n.-27-125_-27-121del
NM_001243786.1:c.-27-125_-27-121del (RAG2) NP_001230715.1:n.-27-125_-27-121del
XM_011519885.1:c.-387_-383del (IFTAP) XP_011518187.1:n.-387_-383del
XM_011519885.3:c.-387_-383del (IFTAP) XP_011518187.1:n.-387_-383del
NM_000536.4:c.-27-125_-27-121del (RAG2) MANE Select NP_000527.2:n.-27-125_-27-121del
NM_001243785.2:c.-27-125_-27-121del (RAG2) NP_001230714.1:n.-27-125_-27-121del
NM_001243786.2:c.-27-125_-27-121del (RAG2) NP_001230715.1:n.-27-125_-27-121del
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