Canonical Allele Identifier: CA352620269

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467562A>T , CM000665.2:g.48467562A>T GRCh38
NC_000003.11:g.48508961A>T , CM000665.1:g.48508961A>T GRCh37
NC_000003.10:g.48483965A>T NCBI36
NG_009820.1:g.6733A>T
NG_033100.1:g.38299T>A
NG_041782.1:g.25853A>T
NG_009820.2:g.6733A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*2008A>T (ATRIP) MANE Select ENSP00000323099.3:n.*2008A>T
ENST00000492235.2:c.490A>T (TREX1) ENSP00000494511.1:p.Thr164Ser
ENST00000625293.3:c.907A>T (TREX1) MANE Select ENSP00000486676.2:p.Thr303Ser
ENST00000634384.2:c.3502A>T (ATRIP)
ENST00000635452.2:c.490A>T (TREX1) ENSP00000492023.2:p.Thr164Ser
ENST00000296443.11:c.907A>T ENSP00000296443.11:p.Thr303Ser
ENST00000433541.1:c.490A>T (TREX1) ENSP00000412404.1:p.Thr164Ser
ENST00000444177.1:c.877A>T (TREX1) ENSP00000415972.1:p.Thr293Ser
ENST00000456089.1:c.490A>T (TREX1) ENSP00000411331.1:p.Thr164Ser
ENST00000625293.1:c.1072A>T (TREX1) ENSP00000486676.1:p.Thr358Ser
ENST00000629913.1:c.907A>T (TREX1) ENSP00000486444.1:p.Thr303Ser
ENST00000634384.1:c.*3727A>T ENSP00000489041.1:n.*3727A>T
ENST00000635452.1:n.2114A>T
ENST00000635464.1:c.3860A>T ENSP00000489199.1:n.3860A>T
NM_007248.3:c.877A>T (TREX1) NP_009179.2:p.Thr293Ser
NM_016381.5:c.1072A>T (TREX1) NP_057465.1:p.Thr358Ser
NM_033629.4:c.907A>T (TREX1) NP_338599.1:p.Thr303Ser
NM_007248.4:c.877A>T (TREX1) NP_009179.2:p.Thr293Ser
NM_033629.5:c.907A>T (TREX1) NP_338599.1:p.Thr303Ser
NR_153405.1:n.4216A>T
NM_033629.6:c.907A>T (TREX1) MANE Select NP_338599.1:p.Thr303Ser
NM_130384.3:c.*2008A>T (ATRIP) MANE Select NP_569055.1:n.*2008A>T
NM_001271023.2:c.*2008A>T (ATRIP) NP_001257952.1:n.*2008A>T
NM_007248.5:c.877A>T (TREX1) NP_009179.2:p.Thr293Ser
NM_032166.4:c.*2008A>T (ATRIP) NP_115542.2:n.*2008A>T
NM_001271022.2:c.*2008A>T (ATRIP) NP_001257951.1:n.*2008A>T