Canonical Allele Identifier: CA352617097

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466732T>A , CM000665.2:g.48466732T>A GRCh38
NC_000003.11:g.48508131T>A , CM000665.1:g.48508131T>A GRCh37
NC_000003.10:g.48483135T>A NCBI36
NG_009820.1:g.5903T>A
NG_033100.1:g.39129A>T
NG_041782.1:g.25023T>A
NG_009820.2:g.5903T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1178T>A (ATRIP) MANE Select ENSP00000323099.3:n.*1178T>A
ENST00000492235.2:c.-295-46T>A (TREX1) ENSP00000494511.1:n.-295-46T>A
ENST00000625293.3:c.77T>A (TREX1) MANE Select ENSP00000486676.2:p.Phe26Tyr
ENST00000634384.2:c.2672T>A (ATRIP)
ENST00000635452.2:c.-333-8T>A (TREX1) ENSP00000492023.2:n.-333-8T>A
ENST00000296443.11:c.77T>A ENSP00000296443.11:p.Phe26Tyr
ENST00000433541.1:c.-333-8T>A (TREX1) ENSP00000412404.1:n.-333-8T>A
ENST00000444177.1:c.47T>A (TREX1) ENSP00000415972.1:p.Phe16Tyr
ENST00000456089.1:c.-8-333T>A (TREX1) ENSP00000411331.1:n.-8-333T>A
ENST00000492235.1:n.41-46T>A (TREX1)
ENST00000625293.1:c.242T>A (TREX1) ENSP00000486676.1:p.Phe81Tyr
ENST00000629913.1:c.77T>A (TREX1) ENSP00000486444.1:p.Phe26Tyr
ENST00000634384.1:c.*2897T>A ENSP00000489041.1:n.*2897T>A
ENST00000635452.1:n.1284T>A
ENST00000635464.1:c.3030T>A ENSP00000489199.1:n.3030T>A
NM_007248.3:c.47T>A (TREX1) NP_009179.2:p.Phe16Tyr
NM_016381.5:c.242T>A (TREX1) NP_057465.1:p.Phe81Tyr
NM_033629.4:c.77T>A (TREX1) NP_338599.1:p.Phe26Tyr
NM_007248.4:c.47T>A (TREX1) NP_009179.2:p.Phe16Tyr
NM_033629.5:c.77T>A (TREX1) NP_338599.1:p.Phe26Tyr
NR_153405.1:n.3386T>A
NM_033629.6:c.77T>A (TREX1) MANE Select NP_338599.1:p.Phe26Tyr
NM_130384.3:c.*1178T>A (ATRIP) MANE Select NP_569055.1:n.*1178T>A
NM_001271023.2:c.*1178T>A (ATRIP) NP_001257952.1:n.*1178T>A
NM_007248.5:c.47T>A (TREX1) NP_009179.2:p.Phe16Tyr
NM_032166.4:c.*1178T>A (ATRIP) NP_115542.2:n.*1178T>A
NM_001271022.2:c.*1178T>A (ATRIP) NP_001257951.1:n.*1178T>A