Canonical Allele Identifier: CA1964210965
Gene: RAG1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36512203G>C , CM000673.2:g.36512203G>C GRCh38
NC_000011.9:g.36533753G>C , CM000673.1:g.36533753G>C GRCh37
NC_000011.8:g.36490329G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000697713.1:c.-131+1666G>C ENSP00000513411.1:n.-131+1666G>C
ENST00000697714.1:c.-15+1666G>C ENSP00000513412.1:n.-15+1666G>C
ENST00000697715.1:c.-289+1666G>C ENSP00000513413.1:n.-289+1666G>C
ENST00000529126.5:n.330+1165G>C
XM_005253041.3:c.-15+1666G>C XP_005253098.1:n.-15+1666G>C
XM_011520250.1:c.-129+1666G>C XP_011518552.1:n.-129+1666G>C
XM_011520251.1:c.-227+1666G>C XP_011518553.1:n.-227+1666G>C
XM_005253041.4:c.-15+1666G>C XP_005253098.1:n.-15+1666G>C
XM_011520250.2:c.-129+1666G>C XP_011518552.1:n.-129+1666G>C
NM_001377277.1:c.-289+1666G>C NP_001364206.1:n.-289+1666G>C
NM_001377278.1:c.-227+1666G>C NP_001364207.1:n.-227+1666G>C
NM_001377279.1:c.-129+1666G>C NP_001364208.1:n.-129+1666G>C
NM_001377280.1:c.-15+1666G>C NP_001364209.1:n.-15+1666G>C
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