Canonical Allele Identifier: CA352618403

Gene: ATRIP TREX1

Linked Data

• MyVariant Identifiers: chr3:g.48508583T>A (hg19) ; chr3:g.48467184T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467184T>A , CM000665.2:g.48467184T>A	GRCh38
NC_000003.11:g.48508583T>A , CM000665.1:g.48508583T>A	GRCh37
NC_000003.10:g.48483587T>A	NCBI36
NG_009820.1:g.6355T>A
NG_033100.1:g.38677A>T
NG_041782.1:g.25475T>A
NG_009820.2:g.6355T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*1630T>A (ATRIP) MANE Select	ENSP00000323099.3:n.*1630T>A
ENST00000492235.2:c.112T>A (TREX1)	ENSP00000494511.1:p.Tyr38Asn
ENST00000625293.3:c.529T>A (TREX1) MANE Select	ENSP00000486676.2:p.Tyr177Asn
ENST00000634384.2:c.3124T>A (ATRIP)
ENST00000635452.2:c.112T>A (TREX1)	ENSP00000492023.2:p.Tyr38Asn
ENST00000296443.11:c.529T>A	ENSP00000296443.11:p.Tyr177Asn
ENST00000433541.1:c.112T>A (TREX1)	ENSP00000412404.1:p.Tyr38Asn
ENST00000444177.1:c.499T>A (TREX1)	ENSP00000415972.1:p.Tyr167Asn
ENST00000456089.1:c.112T>A (TREX1)	ENSP00000411331.1:p.Tyr38Asn
ENST00000492235.1:n.447T>A (TREX1)
ENST00000625293.1:c.694T>A (TREX1)	ENSP00000486676.1:p.Tyr232Asn
ENST00000629913.1:c.529T>A (TREX1)	ENSP00000486444.1:p.Tyr177Asn
ENST00000634384.1:c.*3349T>A	ENSP00000489041.1:n.*3349T>A
ENST00000635452.1:n.1736T>A
ENST00000635464.1:c.3482T>A	ENSP00000489199.1:n.3482T>A
NM_007248.3:c.499T>A (TREX1)	NP_009179.2:p.Tyr167Asn
NM_016381.5:c.694T>A (TREX1)	NP_057465.1:p.Tyr232Asn
NM_033629.4:c.529T>A (TREX1)	NP_338599.1:p.Tyr177Asn
NM_007248.4:c.499T>A (TREX1)	NP_009179.2:p.Tyr167Asn
NM_033629.5:c.529T>A (TREX1)	NP_338599.1:p.Tyr177Asn
NR_153405.1:n.3838T>A
NM_033629.6:c.529T>A (TREX1) MANE Select	NP_338599.1:p.Tyr177Asn
NM_130384.3:c.*1630T>A (ATRIP) MANE Select	NP_569055.1:n.*1630T>A
NM_001271023.2:c.*1630T>A (ATRIP)	NP_001257952.1:n.*1630T>A
NM_007248.5:c.499T>A (TREX1)	NP_009179.2:p.Tyr167Asn
NM_032166.4:c.*1630T>A (ATRIP)	NP_115542.2:n.*1630T>A
NM_001271022.2:c.*1630T>A (ATRIP)	NP_001257951.1:n.*1630T>A