Canonical Allele Identifier: CA2613151059
Gene: RAG2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.36593869del , CM000673.2:g.36593869del GRCh38
NC_000011.9:g.36615419del , CM000673.1:g.36615419del GRCh37
NC_000011.8:g.36571995del NCBI36
NG_007573.1:g.9368del , LRG_99:g.9368del
NG_033154.1:g.4377del

Transcript Alleles

HGVS Amino-acid change
ENST00000527033.6:c.300del ENSP00000436895.2:p.Asn100LysfsTer?
ENST00000529083.2:c.300del ENSP00000436327.2:p.Asn100LysfsTer?
ENST00000532616.2:c.300del ENSP00000432174.2:p.Asn100LysfsTer?
ENST00000311485.8:c.300del MANE Select ENSP00000308620.4:p.Asn100LysfsTer?
ENST00000311485.7:c.300del ENSP00000308620.3:p.Asn100LysfsTer?
ENST00000524423.1:n.131+4233del
ENST00000529083.1:c.300del ENSP00000436327.1:p.Asn100LysfsTer?
ENST00000618712.4:c.300del ENSP00000478672.1:p.Asn100LysfsTer?
NM_000536.3:c.300del NP_000527.2:p.Asn100LysfsTer?
NM_001243785.1:c.300del NP_001230714.1:p.Asn100LysfsTer?
NM_001243786.1:c.300del NP_001230715.1:p.Asn100LysfsTer?
NM_000536.4:c.300del MANE Select NP_000527.2:p.Asn100LysfsTer?
NM_001243785.2:c.300del NP_001230714.1:p.Asn100LysfsTer?
NM_001243786.2:c.300del NP_001230715.1:p.Asn100LysfsTer?