Canonical Allele Identifier: CA433615886

Gene: ATRIP TREX1

Linked Data

• ClinVar Variation Id: 2947393
• ClinVar RCV Id: RCV003801583
• MyVariant Identifiers: chr3:g.48508807T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467408T>G , CM000665.2:g.48467408T>G	GRCh38
NC_000003.11:g.48508807T>G , CM000665.1:g.48508807T>G	GRCh37
NC_000003.10:g.48483811T>G	NCBI36
NG_009820.1:g.6579T>G
NG_033100.1:g.38453A>C
NG_041782.1:g.25699T>G
NG_009820.2:g.6579T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*1854T>G (ATRIP) MANE Select	ENSP00000323099.3:n.*1854T>G
ENST00000492235.2:c.336T>G (TREX1)	ENSP00000494511.1:p.Thr112=
ENST00000625293.3:c.753T>G (TREX1) MANE Select	ENSP00000486676.2:p.Thr251=
ENST00000634384.2:c.3348T>G (ATRIP)
ENST00000635452.2:c.336T>G (TREX1)	ENSP00000492023.2:p.Thr112=
ENST00000296443.11:c.753T>G	ENSP00000296443.11:p.Thr251=
ENST00000433541.1:c.336T>G (TREX1)	ENSP00000412404.1:p.Thr112=
ENST00000444177.1:c.723T>G (TREX1)	ENSP00000415972.1:p.Thr241=
ENST00000456089.1:c.336T>G (TREX1)	ENSP00000411331.1:p.Thr112=
ENST00000492235.1:n.671T>G (TREX1)
ENST00000625293.1:c.918T>G (TREX1)	ENSP00000486676.1:p.Thr306=
ENST00000629913.1:c.753T>G (TREX1)	ENSP00000486444.1:p.Thr251=
ENST00000634384.1:c.*3573T>G	ENSP00000489041.1:n.*3573T>G
ENST00000635452.1:n.1960T>G
ENST00000635464.1:c.3706T>G	ENSP00000489199.1:n.3706T>G
NM_007248.3:c.723T>G (TREX1)	NP_009179.2:p.Thr241=
NM_016381.5:c.918T>G (TREX1)	NP_057465.1:p.Thr306=
NM_033629.4:c.753T>G (TREX1)	NP_338599.1:p.Thr251=
NM_007248.4:c.723T>G (TREX1)	NP_009179.2:p.Thr241=
NM_033629.5:c.753T>G (TREX1)	NP_338599.1:p.Thr251=
NR_153405.1:n.4062T>G
NM_033629.6:c.753T>G (TREX1) MANE Select	NP_338599.1:p.Thr251=
NM_130384.3:c.*1854T>G (ATRIP) MANE Select	NP_569055.1:n.*1854T>G
NM_001271023.2:c.*1854T>G (ATRIP)	NP_001257952.1:n.*1854T>G
NM_007248.5:c.723T>G (TREX1)	NP_009179.2:p.Thr241=
NM_032166.4:c.*1854T>G (ATRIP)	NP_115542.2:n.*1854T>G
NM_001271022.2:c.*1854T>G (ATRIP)	NP_001257951.1:n.*1854T>G