Canonical Allele Identifier: CA352617415

Linked Data

ClinVar Variation Id: 1471811
ClinVar RCV Id: RCV001966962
dbSNP Id: rs2107256110

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466807A>C , CM000665.2:g.48466807A>C GRCh38
NC_000003.11:g.48508206A>C , CM000665.1:g.48508206A>C GRCh37
NC_000003.10:g.48483210A>C NCBI36
NG_009820.1:g.5978A>C
NG_033100.1:g.39054T>G
NG_041782.1:g.25098A>C
NG_009820.2:g.5978A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1253A>C (ATRIP) MANE Select ENSP00000323099.3:n.*1253A>C
ENST00000492235.2:c.-266A>C (TREX1) ENSP00000494511.1:n.-266A>C
ENST00000625293.3:c.152A>C (TREX1) MANE Select ENSP00000486676.2:p.Gln51Pro
ENST00000634384.2:c.2747A>C (ATRIP)
ENST00000635452.2:c.-266A>C (TREX1) ENSP00000492023.2:n.-266A>C
ENST00000296443.11:c.152A>C ENSP00000296443.11:p.Gln51Pro
ENST00000433541.1:c.-266A>C (TREX1) ENSP00000412404.1:n.-266A>C
ENST00000444177.1:c.122A>C (TREX1) ENSP00000415972.1:p.Gln41Pro
ENST00000456089.1:c.-8-258A>C (TREX1) ENSP00000411331.1:n.-8-258A>C
ENST00000492235.1:n.70A>C (TREX1)
ENST00000625293.1:c.317A>C (TREX1) ENSP00000486676.1:p.Gln106Pro
ENST00000629913.1:c.152A>C (TREX1) ENSP00000486444.1:p.Gln51Pro
ENST00000634384.1:c.*2972A>C ENSP00000489041.1:n.*2972A>C
ENST00000635452.1:n.1359A>C
ENST00000635464.1:c.3105A>C ENSP00000489199.1:n.3105A>C
NM_007248.3:c.122A>C (TREX1) NP_009179.2:p.Gln41Pro
NM_016381.5:c.317A>C (TREX1) NP_057465.1:p.Gln106Pro
NM_033629.4:c.152A>C (TREX1) NP_338599.1:p.Gln51Pro
NM_007248.4:c.122A>C (TREX1) NP_009179.2:p.Gln41Pro
NM_033629.5:c.152A>C (TREX1) NP_338599.1:p.Gln51Pro
NR_153405.1:n.3461A>C
NM_033629.6:c.152A>C (TREX1) MANE Select NP_338599.1:p.Gln51Pro
NM_130384.3:c.*1253A>C (ATRIP) MANE Select NP_569055.1:n.*1253A>C
NM_001271023.2:c.*1253A>C (ATRIP) NP_001257952.1:n.*1253A>C
NM_007248.5:c.122A>C (TREX1) NP_009179.2:p.Gln41Pro
NM_032166.4:c.*1253A>C (ATRIP) NP_115542.2:n.*1253A>C
NM_001271022.2:c.*1253A>C (ATRIP) NP_001257951.1:n.*1253A>C