Canonical Allele Identifier: CA2573146311

Gene: RAG2

Linked Data

• ClinVar Variation Id: 1457376
• ClinVar RCV Id: RCV001949224
• dbSNP Id: rs2133314424

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36593635del , CM000673.2:g.36593635del	GRCh38
NC_000011.9:g.36615185del , CM000673.1:g.36615185del	GRCh37
NC_000011.8:g.36571761del	NCBI36
NG_007573.1:g.9603del , LRG_99:g.9603del
NG_033154.1:g.4143del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.535del	ENSP00000436895.2:p.Leu179CysfsTer?
ENST00000529083.2:c.535del	ENSP00000436327.2:p.Leu179CysfsTer?
ENST00000532616.2:c.535del	ENSP00000432174.2:p.Leu179CysfsTer?
ENST00000311485.8:c.535del MANE Select	ENSP00000308620.4:p.Leu179CysfsTer?
ENST00000311485.7:c.535del	ENSP00000308620.3:p.Leu179CysfsTer?
ENST00000524423.1:n.131+4468del
ENST00000618712.4:c.535del	ENSP00000478672.1:p.Leu179CysfsTer?
NM_000536.3:c.535del	NP_000527.2:p.Leu179CysfsTer?
NM_001243785.1:c.535del	NP_001230714.1:p.Leu179CysfsTer?
NM_001243786.1:c.535del	NP_001230715.1:p.Leu179CysfsTer?
NM_000536.4:c.535del MANE Select	NP_000527.2:p.Leu179CysfsTer?
NM_001243785.2:c.535del	NP_001230714.1:p.Leu179CysfsTer?
NM_001243786.2:c.535del	NP_001230715.1:p.Leu179CysfsTer?