Canonical Allele Identifier: CA2613151054

Gene: RAG2

Linked Data

• gnomAD v4: 11-36593540-A-AT

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36593541dup , CM000673.2:g.36593541dup	GRCh38
NC_000011.9:g.36615091dup , CM000673.1:g.36615091dup	GRCh37
NC_000011.8:g.36571667dup	NCBI36
NG_007573.1:g.9696dup , LRG_99:g.9696dup
NG_033154.1:g.4049dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000527033.6:c.628dup	ENSP00000436895.2:p.Ile210AsnfsTer5
ENST00000529083.2:c.628dup	ENSP00000436327.2:p.Ile210AsnfsTer5
ENST00000532616.2:c.628dup	ENSP00000432174.2:p.Ile210AsnfsTer5
ENST00000311485.8:c.628dup MANE Select	ENSP00000308620.4:p.Ile210AsnfsTer5
ENST00000311485.7:c.628dup	ENSP00000308620.3:p.Ile210AsnfsTer5
ENST00000524423.1:n.131+4561dup
ENST00000618712.4:c.628dup	ENSP00000478672.1:p.Ile210AsnfsTer5
NM_000536.3:c.628dup	NP_000527.2:p.Ile210AsnfsTer5
NM_001243785.1:c.628dup	NP_001230714.1:p.Ile210AsnfsTer5
NM_001243786.1:c.628dup	NP_001230715.1:p.Ile210AsnfsTer5
NM_000536.4:c.628dup MANE Select	NP_000527.2:p.Ile210AsnfsTer5
NM_001243785.2:c.628dup	NP_001230714.1:p.Ile210AsnfsTer5
NM_001243786.2:c.628dup	NP_001230715.1:p.Ile210AsnfsTer5