Canonical Allele Identifier: CA73933304

Gene: ATRIP TREX1

Linked Data

• ClinVar Variation Id: 1554349
• ClinVar RCV Id: RCV002199607 ; RCV003438926
• dbSNP Id: rs149654159
• gnomAD v2: 3-48508882-G-A
• gnomAD v3: 3-48467483-G-A
• gnomAD v4: 3-48467483-G-A
• MyVariant Identifiers: chr3:g.48508882G>A (hg19) ; chr3:g.48467483G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467483G>A , CM000665.2:g.48467483G>A	GRCh38
NC_000003.11:g.48508882G>A , CM000665.1:g.48508882G>A	GRCh37
NC_000003.10:g.48483886G>A	NCBI36
NG_009820.1:g.6654G>A
NG_033100.1:g.38378C>T
NG_041782.1:g.25774G>A
NG_009820.2:g.6654G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*1929G>A (ATRIP) MANE Select	ENSP00000323099.3:n.*1929G>A
ENST00000492235.2:c.411G>A (TREX1)	ENSP00000494511.1:p.Val137=
ENST00000625293.3:c.828G>A (TREX1) MANE Select	ENSP00000486676.2:p.Val276=
ENST00000634384.2:c.3423G>A (ATRIP)
ENST00000635452.2:c.411G>A (TREX1)	ENSP00000492023.2:p.Val137=
ENST00000296443.11:c.828G>A	ENSP00000296443.11:p.Val276=
ENST00000433541.1:c.411G>A (TREX1)	ENSP00000412404.1:p.Val137=
ENST00000444177.1:c.798G>A (TREX1)	ENSP00000415972.1:p.Val266=
ENST00000456089.1:c.411G>A (TREX1)	ENSP00000411331.1:p.Val137=
ENST00000625293.1:c.993G>A (TREX1)	ENSP00000486676.1:p.Val331=
ENST00000629913.1:c.828G>A (TREX1)	ENSP00000486444.1:p.Val276=
ENST00000634384.1:c.*3648G>A	ENSP00000489041.1:n.*3648G>A
ENST00000635452.1:n.2035G>A
ENST00000635464.1:c.3781G>A	ENSP00000489199.1:n.3781G>A
NM_007248.3:c.798G>A (TREX1)	NP_009179.2:p.Val266=
NM_016381.5:c.993G>A (TREX1)	NP_057465.1:p.Val331=
NM_033629.4:c.828G>A (TREX1)	NP_338599.1:p.Val276=
NM_007248.4:c.798G>A (TREX1)	NP_009179.2:p.Val266=
NM_033629.5:c.828G>A (TREX1)	NP_338599.1:p.Val276=
NR_153405.1:n.4137G>A
NM_033629.6:c.828G>A (TREX1) MANE Select	NP_338599.1:p.Val276=
NM_130384.3:c.*1929G>A (ATRIP) MANE Select	NP_569055.1:n.*1929G>A
NM_001271023.2:c.*1929G>A (ATRIP)	NP_001257952.1:n.*1929G>A
NM_007248.5:c.798G>A (TREX1)	NP_009179.2:p.Val266=
NM_032166.4:c.*1929G>A (ATRIP)	NP_115542.2:n.*1929G>A
NM_001271022.2:c.*1929G>A (ATRIP)	NP_001257951.1:n.*1929G>A