Canonical Allele Identifier: CA433615931

Gene: ATRIP TREX1

Linked Data

• ClinVar Variation Id: 1633336
• ClinVar RCV Id: RCV002142602
• dbSNP Id: rs2107261127
• MyVariant Identifiers: chr3:g.48508612G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467213G>A , CM000665.2:g.48467213G>A	GRCh38
NC_000003.11:g.48508612G>A , CM000665.1:g.48508612G>A	GRCh37
NC_000003.10:g.48483616G>A	NCBI36
NG_009820.1:g.6384G>A
NG_033100.1:g.38648C>T
NG_041782.1:g.25504G>A
NG_009820.2:g.6384G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*1659G>A (ATRIP) MANE Select	ENSP00000323099.3:n.*1659G>A
ENST00000492235.2:c.141G>A (TREX1)	ENSP00000494511.1:p.Leu47=
ENST00000625293.3:c.558G>A (TREX1) MANE Select	ENSP00000486676.2:p.Leu186=
ENST00000634384.2:c.3153G>A (ATRIP)
ENST00000635452.2:c.141G>A (TREX1)	ENSP00000492023.2:p.Leu47=
ENST00000296443.11:c.558G>A	ENSP00000296443.11:p.Leu186=
ENST00000433541.1:c.141G>A (TREX1)	ENSP00000412404.1:p.Leu47=
ENST00000444177.1:c.528G>A (TREX1)	ENSP00000415972.1:p.Leu176=
ENST00000456089.1:c.141G>A (TREX1)	ENSP00000411331.1:p.Leu47=
ENST00000492235.1:n.476G>A (TREX1)
ENST00000625293.1:c.723G>A (TREX1)	ENSP00000486676.1:p.Leu241=
ENST00000629913.1:c.558G>A (TREX1)	ENSP00000486444.1:p.Leu186=
ENST00000634384.1:c.*3378G>A	ENSP00000489041.1:n.*3378G>A
ENST00000635452.1:n.1765G>A
ENST00000635464.1:c.3511G>A	ENSP00000489199.1:n.3511G>A
NM_007248.3:c.528G>A (TREX1)	NP_009179.2:p.Leu176=
NM_016381.5:c.723G>A (TREX1)	NP_057465.1:p.Leu241=
NM_033629.4:c.558G>A (TREX1)	NP_338599.1:p.Leu186=
NM_007248.4:c.528G>A (TREX1)	NP_009179.2:p.Leu176=
NM_033629.5:c.558G>A (TREX1)	NP_338599.1:p.Leu186=
NR_153405.1:n.3867G>A
NM_033629.6:c.558G>A (TREX1) MANE Select	NP_338599.1:p.Leu186=
NM_130384.3:c.*1659G>A (ATRIP) MANE Select	NP_569055.1:n.*1659G>A
NM_001271023.2:c.*1659G>A (ATRIP)	NP_001257952.1:n.*1659G>A
NM_007248.5:c.528G>A (TREX1)	NP_009179.2:p.Leu176=
NM_032166.4:c.*1659G>A (ATRIP)	NP_115542.2:n.*1659G>A
NM_001271022.2:c.*1659G>A (ATRIP)	NP_001257951.1:n.*1659G>A