Canonical Allele Identifier: CA380150511
Gene: RAG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.36595760C>G (hg19) chr11:g.36574210C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36574210C>G , CM000673.2:g.36574210C>G GRCh38
NC_000011.9:g.36595760C>G , CM000673.1:g.36595760C>G GRCh37
NC_000011.8:g.36552336C>G NCBI36
NG_007528.1:g.11198C>G , LRG_98:g.11198C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000697713.1:c.906C>G ENSP00000513411.1:p.Asp302Glu
ENST00000697714.1:c.906C>G ENSP00000513412.1:p.Asp302Glu
ENST00000697715.1:c.906C>G ENSP00000513413.1:p.Asp302Glu
ENST00000299440.6:c.906C>G MANE Select ENSP00000299440.5:p.Asp302Glu
ENST00000299440.5:c.906C>G ENSP00000299440.5:p.Asp302Glu
ENST00000534663.1:c.906C>G ENSP00000434610.1:p.Asp302Glu
NM_000448.2:c.906C>G , LRG_98t1:c.906C>G NP_000439.1:p.Asp302Glu
XM_005253041.3:c.906C>G XP_005253098.1:p.Asp302Glu
XM_011520250.1:c.906C>G XP_011518552.1:p.Asp302Glu
XM_011520251.1:c.906C>G XP_011518553.1:p.Asp302Glu
XM_005253041.4:c.906C>G XP_005253098.1:p.Asp302Glu
XM_011520250.2:c.906C>G XP_011518552.1:p.Asp302Glu
NM_000448.3:c.906C>G MANE Select NP_000439.2:p.Asp302Glu
NM_001377277.1:c.906C>G NP_001364206.1:p.Asp302Glu
NM_001377278.1:c.906C>G NP_001364207.1:p.Asp302Glu
NM_001377279.1:c.906C>G NP_001364208.1:p.Asp302Glu
NM_001377280.1:c.906C>G NP_001364209.1:p.Asp302Glu
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