Canonical Allele Identifier: CA1964192321

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36592580_36592581delinsCA , CM000673.2:g.36592580_36592581delinsCA GRCh38
NC_000011.9:g.36614130_36614131delinsCA , CM000673.1:g.36614130_36614131delinsCA GRCh37
NC_000011.8:g.36570706_36570707delinsCA NCBI36
NG_007573.1:g.10656_10657delinsTG , LRG_99:g.10656_10657delinsTG
NG_033154.1:g.3088_3089delinsCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000311485.8:c.*4_*5delinsTG (RAG2) MANE Select ENSP00000308620.4:n.*4_*5delinsTG
ENST00000311485.7:c.*4_*5delinsTG (RAG2) ENSP00000308620.3:n.*4_*5delinsTG
ENST00000524423.1:n.131+5521_131+5522delinsTG (RAG2)
ENST00000534663.1:c.*86-387_*86-386delinsCA (RAG1) ENSP00000434610.1:n.*86-387_*86-386delinsCA
ENST00000618712.4:c.*4_*5delinsTG (RAG2) ENSP00000478672.1:n.*4_*5delinsTG
NM_000536.3:c.*4_*5delinsTG (RAG2) NP_000527.2:n.*4_*5delinsTG
NM_001243785.1:c.*4_*5delinsTG (RAG2) NP_001230714.1:n.*4_*5delinsTG
NM_001243786.1:c.*4_*5delinsTG (RAG2) NP_001230715.1:n.*4_*5delinsTG
NM_000536.4:c.*4_*5delinsTG (RAG2) MANE Select NP_000527.2:n.*4_*5delinsTG
NM_001243785.2:c.*4_*5delinsTG (RAG2) NP_001230714.1:n.*4_*5delinsTG
NM_001243786.2:c.*4_*5delinsTG (RAG2) NP_001230715.1:n.*4_*5delinsTG