Canonical Allele Identifier: CA352619933

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467500T>C , CM000665.2:g.48467500T>C GRCh38
NC_000003.11:g.48508899T>C , CM000665.1:g.48508899T>C GRCh37
NC_000003.10:g.48483903T>C NCBI36
NG_009820.1:g.6671T>C
NG_033100.1:g.38361A>G
NG_041782.1:g.25791T>C
NG_009820.2:g.6671T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1946T>C (ATRIP) MANE Select ENSP00000323099.3:n.*1946T>C
ENST00000492235.2:c.428T>C (TREX1) ENSP00000494511.1:p.Leu143Pro
ENST00000625293.3:c.845T>C (TREX1) MANE Select ENSP00000486676.2:p.Leu282Pro
ENST00000634384.2:c.3440T>C (ATRIP)
ENST00000635452.2:c.428T>C (TREX1) ENSP00000492023.2:p.Leu143Pro
ENST00000296443.11:c.845T>C ENSP00000296443.11:p.Leu282Pro
ENST00000433541.1:c.428T>C (TREX1) ENSP00000412404.1:p.Leu143Pro
ENST00000444177.1:c.815T>C (TREX1) ENSP00000415972.1:p.Leu272Pro
ENST00000456089.1:c.428T>C (TREX1) ENSP00000411331.1:p.Leu143Pro
ENST00000625293.1:c.1010T>C (TREX1) ENSP00000486676.1:p.Leu337Pro
ENST00000629913.1:c.845T>C (TREX1) ENSP00000486444.1:p.Leu282Pro
ENST00000634384.1:c.*3665T>C ENSP00000489041.1:n.*3665T>C
ENST00000635452.1:n.2052T>C
ENST00000635464.1:c.3798T>C ENSP00000489199.1:n.3798T>C
NM_007248.3:c.815T>C (TREX1) NP_009179.2:p.Leu272Pro
NM_016381.5:c.1010T>C (TREX1) NP_057465.1:p.Leu337Pro
NM_033629.4:c.845T>C (TREX1) NP_338599.1:p.Leu282Pro
NM_007248.4:c.815T>C (TREX1) NP_009179.2:p.Leu272Pro
NM_033629.5:c.845T>C (TREX1) NP_338599.1:p.Leu282Pro
NR_153405.1:n.4154T>C
NM_033629.6:c.845T>C (TREX1) MANE Select NP_338599.1:p.Leu282Pro
NM_130384.3:c.*1946T>C (ATRIP) MANE Select NP_569055.1:n.*1946T>C
NM_001271023.2:c.*1946T>C (ATRIP) NP_001257952.1:n.*1946T>C
NM_007248.5:c.815T>C (TREX1) NP_009179.2:p.Leu272Pro
NM_032166.4:c.*1946T>C (ATRIP) NP_115542.2:n.*1946T>C
NM_001271022.2:c.*1946T>C (ATRIP) NP_001257951.1:n.*1946T>C