Canonical Allele Identifier: CA352619024

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467345G>T , CM000665.2:g.48467345G>T GRCh38
NC_000003.11:g.48508744G>T , CM000665.1:g.48508744G>T GRCh37
NC_000003.10:g.48483748G>T NCBI36
NG_009820.1:g.6516G>T
NG_033100.1:g.38516C>A
NG_041782.1:g.25636G>T
NG_009820.2:g.6516G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1791G>T (ATRIP) MANE Select ENSP00000323099.3:n.*1791G>T
ENST00000492235.2:c.273G>T (TREX1) ENSP00000494511.1:p.Arg91Ser
ENST00000625293.3:c.690G>T (TREX1) MANE Select ENSP00000486676.2:p.Arg230Ser
ENST00000634384.2:c.3285G>T (ATRIP)
ENST00000635452.2:c.273G>T (TREX1) ENSP00000492023.2:p.Arg91Ser
ENST00000296443.11:c.690G>T ENSP00000296443.11:p.Arg230Ser
ENST00000433541.1:c.273G>T (TREX1) ENSP00000412404.1:p.Arg91Ser
ENST00000444177.1:c.660G>T (TREX1) ENSP00000415972.1:p.Arg220Ser
ENST00000456089.1:c.273G>T (TREX1) ENSP00000411331.1:p.Arg91Ser
ENST00000492235.1:n.608G>T (TREX1)
ENST00000625293.1:c.855G>T (TREX1) ENSP00000486676.1:p.Arg285Ser
ENST00000629913.1:c.690G>T (TREX1) ENSP00000486444.1:p.Arg230Ser
ENST00000634384.1:c.*3510G>T ENSP00000489041.1:n.*3510G>T
ENST00000635452.1:n.1897G>T
ENST00000635464.1:c.3643G>T ENSP00000489199.1:n.3643G>T
NM_007248.3:c.660G>T (TREX1) NP_009179.2:p.Arg220Ser
NM_016381.5:c.855G>T (TREX1) NP_057465.1:p.Arg285Ser
NM_033629.4:c.690G>T (TREX1) NP_338599.1:p.Arg230Ser
NM_007248.4:c.660G>T (TREX1) NP_009179.2:p.Arg220Ser
NM_033629.5:c.690G>T (TREX1) NP_338599.1:p.Arg230Ser
NR_153405.1:n.3999G>T
NM_033629.6:c.690G>T (TREX1) MANE Select NP_338599.1:p.Arg230Ser
NM_130384.3:c.*1791G>T (ATRIP) MANE Select NP_569055.1:n.*1791G>T
NM_001271023.2:c.*1791G>T (ATRIP) NP_001257952.1:n.*1791G>T
NM_007248.5:c.660G>T (TREX1) NP_009179.2:p.Arg220Ser
NM_032166.4:c.*1791G>T (ATRIP) NP_115542.2:n.*1791G>T
NM_001271022.2:c.*1791G>T (ATRIP) NP_001257951.1:n.*1791G>T