Canonical Allele Identifier: CA352617266

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466771T>A , CM000665.2:g.48466771T>A GRCh38
NC_000003.11:g.48508170T>A , CM000665.1:g.48508170T>A GRCh37
NC_000003.10:g.48483174T>A NCBI36
NG_009820.1:g.5942T>A
NG_033100.1:g.39090A>T
NG_041782.1:g.25062T>A
NG_009820.2:g.5942T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1217T>A (ATRIP) MANE Select ENSP00000323099.3:n.*1217T>A
ENST00000492235.2:c.-295-7T>A (TREX1) ENSP00000494511.1:n.-295-7T>A
ENST00000625293.3:c.116T>A (TREX1) MANE Select ENSP00000486676.2:p.Val39Asp
ENST00000634384.2:c.2711T>A (ATRIP)
ENST00000635452.2:c.-302T>A (TREX1) ENSP00000492023.2:n.-302T>A
ENST00000296443.11:c.116T>A ENSP00000296443.11:p.Val39Asp
ENST00000433541.1:c.-302T>A (TREX1) ENSP00000412404.1:n.-302T>A
ENST00000444177.1:c.86T>A (TREX1) ENSP00000415972.1:p.Val29Asp
ENST00000456089.1:c.-8-294T>A (TREX1) ENSP00000411331.1:n.-8-294T>A
ENST00000492235.1:n.41-7T>A (TREX1)
ENST00000625293.1:c.281T>A (TREX1) ENSP00000486676.1:p.Val94Asp
ENST00000629913.1:c.116T>A (TREX1) ENSP00000486444.1:p.Val39Asp
ENST00000634384.1:c.*2936T>A ENSP00000489041.1:n.*2936T>A
ENST00000635452.1:n.1323T>A
ENST00000635464.1:c.3069T>A ENSP00000489199.1:n.3069T>A
NM_007248.3:c.86T>A (TREX1) NP_009179.2:p.Val29Asp
NM_016381.5:c.281T>A (TREX1) NP_057465.1:p.Val94Asp
NM_033629.4:c.116T>A (TREX1) NP_338599.1:p.Val39Asp
NM_007248.4:c.86T>A (TREX1) NP_009179.2:p.Val29Asp
NM_033629.5:c.116T>A (TREX1) NP_338599.1:p.Val39Asp
NR_153405.1:n.3425T>A
NM_033629.6:c.116T>A (TREX1) MANE Select NP_338599.1:p.Val39Asp
NM_130384.3:c.*1217T>A (ATRIP) MANE Select NP_569055.1:n.*1217T>A
NM_001271023.2:c.*1217T>A (ATRIP) NP_001257952.1:n.*1217T>A
NM_007248.5:c.86T>A (TREX1) NP_009179.2:p.Val29Asp
NM_032166.4:c.*1217T>A (ATRIP) NP_115542.2:n.*1217T>A
NM_001271022.2:c.*1217T>A (ATRIP) NP_001257951.1:n.*1217T>A