Canonical Allele Identifier: CA352617137

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466740C>A , CM000665.2:g.48466740C>A GRCh38
NC_000003.11:g.48508139C>A , CM000665.1:g.48508139C>A GRCh37
NC_000003.10:g.48483143C>A NCBI36
NG_009820.1:g.5911C>A
NG_033100.1:g.39121G>T
NG_041782.1:g.25031C>A
NG_009820.2:g.5911C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1186C>A (ATRIP) MANE Select ENSP00000323099.3:n.*1186C>A
ENST00000492235.2:c.-295-38C>A (TREX1) ENSP00000494511.1:n.-295-38C>A
ENST00000625293.3:c.85C>A (TREX1) MANE Select ENSP00000486676.2:p.Pro29Thr
ENST00000634384.2:c.2680C>A (ATRIP)
ENST00000635452.2:c.-333C>A (TREX1) ENSP00000492023.2:n.-333C>A
ENST00000296443.11:c.85C>A ENSP00000296443.11:p.Pro29Thr
ENST00000433541.1:c.-333C>A (TREX1) ENSP00000412404.1:n.-333C>A
ENST00000444177.1:c.55C>A (TREX1) ENSP00000415972.1:p.Pro19Thr
ENST00000456089.1:c.-8-325C>A (TREX1) ENSP00000411331.1:n.-8-325C>A
ENST00000492235.1:n.41-38C>A (TREX1)
ENST00000625293.1:c.250C>A (TREX1) ENSP00000486676.1:p.Pro84Thr
ENST00000629913.1:c.85C>A (TREX1) ENSP00000486444.1:p.Pro29Thr
ENST00000634384.1:c.*2905C>A ENSP00000489041.1:n.*2905C>A
ENST00000635452.1:n.1292C>A
ENST00000635464.1:c.3038C>A ENSP00000489199.1:n.3038C>A
NM_007248.3:c.55C>A (TREX1) NP_009179.2:p.Pro19Thr
NM_016381.5:c.250C>A (TREX1) NP_057465.1:p.Pro84Thr
NM_033629.4:c.85C>A (TREX1) NP_338599.1:p.Pro29Thr
NM_007248.4:c.55C>A (TREX1) NP_009179.2:p.Pro19Thr
NM_033629.5:c.85C>A (TREX1) NP_338599.1:p.Pro29Thr
NR_153405.1:n.3394C>A
NM_033629.6:c.85C>A (TREX1) MANE Select NP_338599.1:p.Pro29Thr
NM_130384.3:c.*1186C>A (ATRIP) MANE Select NP_569055.1:n.*1186C>A
NM_001271023.2:c.*1186C>A (ATRIP) NP_001257952.1:n.*1186C>A
NM_007248.5:c.55C>A (TREX1) NP_009179.2:p.Pro19Thr
NM_032166.4:c.*1186C>A (ATRIP) NP_115542.2:n.*1186C>A
NM_001271022.2:c.*1186C>A (ATRIP) NP_001257951.1:n.*1186C>A