Canonical Allele Identifier: CA352618996

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467341T>C , CM000665.2:g.48467341T>C GRCh38
NC_000003.11:g.48508740T>C , CM000665.1:g.48508740T>C GRCh37
NC_000003.10:g.48483744T>C NCBI36
NG_009820.1:g.6512T>C
NG_033100.1:g.38520A>G
NG_041782.1:g.25632T>C
NG_009820.2:g.6512T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1787T>C (ATRIP) MANE Select ENSP00000323099.3:n.*1787T>C
ENST00000492235.2:c.269T>C (TREX1) ENSP00000494511.1:p.Ile90Thr
ENST00000625293.3:c.686T>C (TREX1) MANE Select ENSP00000486676.2:p.Ile229Thr
ENST00000634384.2:c.3281T>C (ATRIP)
ENST00000635452.2:c.269T>C (TREX1) ENSP00000492023.2:p.Ile90Thr
ENST00000296443.11:c.686T>C ENSP00000296443.11:p.Ile229Thr
ENST00000433541.1:c.269T>C (TREX1) ENSP00000412404.1:p.Ile90Thr
ENST00000444177.1:c.656T>C (TREX1) ENSP00000415972.1:p.Ile219Thr
ENST00000456089.1:c.269T>C (TREX1) ENSP00000411331.1:p.Ile90Thr
ENST00000492235.1:n.604T>C (TREX1)
ENST00000625293.1:c.851T>C (TREX1) ENSP00000486676.1:p.Ile284Thr
ENST00000629913.1:c.686T>C (TREX1) ENSP00000486444.1:p.Ile229Thr
ENST00000634384.1:c.*3506T>C ENSP00000489041.1:n.*3506T>C
ENST00000635452.1:n.1893T>C
ENST00000635464.1:c.3639T>C ENSP00000489199.1:n.3639T>C
NM_007248.3:c.656T>C (TREX1) NP_009179.2:p.Ile219Thr
NM_016381.5:c.851T>C (TREX1) NP_057465.1:p.Ile284Thr
NM_033629.4:c.686T>C (TREX1) NP_338599.1:p.Ile229Thr
NM_007248.4:c.656T>C (TREX1) NP_009179.2:p.Ile219Thr
NM_033629.5:c.686T>C (TREX1) NP_338599.1:p.Ile229Thr
NR_153405.1:n.3995T>C
NM_033629.6:c.686T>C (TREX1) MANE Select NP_338599.1:p.Ile229Thr
NM_130384.3:c.*1787T>C (ATRIP) MANE Select NP_569055.1:n.*1787T>C
NM_001271023.2:c.*1787T>C (ATRIP) NP_001257952.1:n.*1787T>C
NM_007248.5:c.656T>C (TREX1) NP_009179.2:p.Ile219Thr
NM_032166.4:c.*1787T>C (ATRIP) NP_115542.2:n.*1787T>C
NM_001271022.2:c.*1787T>C (ATRIP) NP_001257951.1:n.*1787T>C