Canonical Allele Identifier: CA474032327
Gene: RAG1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr11:g.36597023T>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36575473T>C , CM000673.2:g.36575473T>C GRCh38
NC_000011.9:g.36597023T>C , CM000673.1:g.36597023T>C GRCh37
NC_000011.8:g.36553599T>C NCBI36
NG_007528.1:g.12461T>C , LRG_98:g.12461T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000697713.1:c.2169T>C ENSP00000513411.1:p.Ala723=
ENST00000697714.1:c.2169T>C ENSP00000513412.1:p.Ala723=
ENST00000697715.1:c.2169T>C ENSP00000513413.1:p.Ala723=
ENST00000299440.6:c.2169T>C MANE Select ENSP00000299440.5:p.Ala723=
ENST00000299440.5:c.2169T>C ENSP00000299440.5:p.Ala723=
ENST00000534663.1:c.2169T>C ENSP00000434610.1:p.Ala723=
NM_000448.2:c.2169T>C , LRG_98t1:c.2169T>C NP_000439.1:p.Ala723=
XM_005253041.3:c.2169T>C XP_005253098.1:p.Ala723=
XM_011520250.1:c.2169T>C XP_011518552.1:p.Ala723=
XM_011520251.1:c.2169T>C XP_011518553.1:p.Ala723=
XM_005253041.4:c.2169T>C XP_005253098.1:p.Ala723=
XM_011520250.2:c.2169T>C XP_011518552.1:p.Ala723=
NM_000448.3:c.2169T>C MANE Select NP_000439.2:p.Ala723=
NM_001377277.1:c.2169T>C NP_001364206.1:p.Ala723=
NM_001377278.1:c.2169T>C NP_001364207.1:p.Ala723=
NM_001377279.1:c.2169T>C NP_001364208.1:p.Ala723=
NM_001377280.1:c.2169T>C NP_001364209.1:p.Ala723=
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