Canonical Allele Identifier: CA1964168693
Community Standard Title: NM_000448.3(RAG1):c.2735A= (p.Tyr912=)

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36576039A= , CM000673.2:g.36576039A= GRCh38
NC_000011.9:g.36597589A= , CM000673.1:g.36597589A= GRCh37
NC_000011.8:g.36554165A= NCBI36
NG_007528.1:g.13027A= , LRG_98:g.13027A=

Transcript Alleles

HGVS Amino-acid Change
NM_000448.3:c.2735A= (RAG1) MANE Select NP_000439.2:p.Tyr912=
ENST00000299440.6:c.2735A= (RAG1) MANE Select ENSP00000299440.5:p.Tyr912=
NM_000448.2:c.2735A= , LRG_98t1:c.2735A= (RAG1) NP_000439.1:p.Tyr912=
NM_001377277.1:c.2735A= (RAG1) NP_001364206.1:p.Tyr912=
NM_001377278.1:c.2735A= (RAG1) NP_001364207.1:p.Tyr912=
NM_001377279.1:c.2735A= (RAG1) NP_001364208.1:p.Tyr912=
NM_001377280.1:c.2735A= (RAG1) NP_001364209.1:p.Tyr912=
ENST00000299440.5:c.2735A= (RAG1) ENSP00000299440.5:p.Tyr912=
ENST00000524423.1:n.132-68T= (RAG2)
ENST00000534663.1:c.2735A= (RAG1) ENSP00000434610.1:p.Tyr912=
ENST00000697713.1:c.2735A= (RAG1) ENSP00000513411.1:p.Tyr912=
ENST00000697714.1:c.2735A= (RAG1) ENSP00000513412.1:p.Tyr912=
ENST00000697715.1:c.2735A= (RAG1) ENSP00000513413.1:p.Tyr912=
XM_005253041.3:c.2735A= (RAG1) XP_005253098.1:p.Tyr912=
XM_005253041.4:c.2735A= (RAG1) XP_005253098.1:p.Tyr912=
XM_011520250.1:c.2735A= (RAG1) XP_011518552.1:p.Tyr912=
XM_011520250.2:c.2735A= (RAG1) XP_011518552.1:p.Tyr912=
XM_011520251.1:c.2735A= (RAG1) XP_011518553.1:p.Tyr912=