Canonical Allele Identifier: CA2613150985

Gene: RAG1

Linked Data

• gnomAD v4: 11-36574998-CTTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.36574999_36575001del , CM000673.2:g.36574999_36575001del	GRCh38
NC_000011.9:g.36596549_36596551del , CM000673.1:g.36596549_36596551del	GRCh37
NC_000011.8:g.36553125_36553127del	NCBI36
NG_007528.1:g.11987_11989del , LRG_98:g.11987_11989del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697713.1:c.1695_1697del	ENSP00000513411.1:p.Leu566del
ENST00000697714.1:c.1695_1697del	ENSP00000513412.1:p.Leu566del
ENST00000697715.1:c.1695_1697del	ENSP00000513413.1:p.Leu566del
ENST00000299440.6:c.1695_1697del MANE Select	ENSP00000299440.5:p.Leu566del
ENST00000299440.5:c.1695_1697del	ENSP00000299440.5:p.Leu566del
ENST00000534663.1:c.1695_1697del	ENSP00000434610.1:p.Leu566del
NM_000448.2:c.1695_1697del , LRG_98t1:c.1695_1697del	NP_000439.1:p.Leu566del
XM_005253041.3:c.1695_1697del	XP_005253098.1:p.Leu566del
XM_011520250.1:c.1695_1697del	XP_011518552.1:p.Leu566del
XM_011520251.1:c.1695_1697del	XP_011518553.1:p.Leu566del
XM_005253041.4:c.1695_1697del	XP_005253098.1:p.Leu566del
XM_011520250.2:c.1695_1697del	XP_011518552.1:p.Leu566del
NM_000448.3:c.1695_1697del MANE Select	NP_000439.2:p.Leu566del
NM_001377277.1:c.1695_1697del	NP_001364206.1:p.Leu566del
NM_001377278.1:c.1695_1697del	NP_001364207.1:p.Leu566del
NM_001377279.1:c.1695_1697del	NP_001364208.1:p.Leu566del
NM_001377280.1:c.1695_1697del	NP_001364209.1:p.Leu566del