Canonical Allele Identifier: CA352616787

Linked Data

ClinVar Variation Id: 1366935
ClinVar RCV Id: RCV001962187
dbSNP Id: rs1179208432
gnomAD v4: 3-48466657-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466657T>C , CM000665.2:g.48466657T>C GRCh38
NC_000003.11:g.48508056T>C , CM000665.1:g.48508056T>C GRCh37
NC_000003.10:g.48483060T>C NCBI36
NG_009820.1:g.5828T>C
NG_033100.1:g.39204A>G
NG_041782.1:g.24948T>C
NG_009820.2:g.5828T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1103T>C (ATRIP) MANE Select ENSP00000323099.3:n.*1103T>C
ENST00000492235.2:c.-295-121T>C (TREX1) ENSP00000494511.1:n.-295-121T>C
ENST00000625293.3:c.2T>C (TREX1) MANE Select ENSP00000486676.2:p.Met1Thr
ENST00000634384.2:c.2597T>C (ATRIP)
ENST00000635452.2:c.-333-83T>C (TREX1) ENSP00000492023.2:n.-333-83T>C
ENST00000296443.11:c.2T>C ENSP00000296443.11:p.Met1Thr
ENST00000433541.1:c.-334+16T>C (TREX1) ENSP00000412404.1:n.-334+16T>C
ENST00000444177.1:c.-18-11T>C (TREX1) ENSP00000415972.1:n.-18-11T>C
ENST00000456089.1:c.-9+348T>C (TREX1) ENSP00000411331.1:n.-9+348T>C
ENST00000492235.1:n.41-121T>C (TREX1)
ENST00000625293.1:c.167T>C (TREX1) ENSP00000486676.1:p.Met56Thr
ENST00000629913.1:c.2T>C (TREX1) ENSP00000486444.1:p.Met1Thr
ENST00000634384.1:c.*2822T>C ENSP00000489041.1:n.*2822T>C
ENST00000635452.1:n.1209T>C
ENST00000635464.1:c.2955T>C ENSP00000489199.1:n.2955T>C
NM_007248.3:c.-18-11T>C (TREX1) NP_009179.2:n.-18-11T>C
NM_016381.5:c.167T>C (TREX1) NP_057465.1:p.Met56Thr
NM_033629.4:c.2T>C (TREX1) NP_338599.1:p.Met1Thr
NM_007248.4:c.-18-11T>C (TREX1) NP_009179.2:n.-18-11T>C
NM_033629.5:c.2T>C (TREX1) NP_338599.1:p.Met1Thr
NR_153405.1:n.3311T>C
NM_033629.6:c.2T>C (TREX1) MANE Select NP_338599.1:p.Met1Thr
NM_130384.3:c.*1103T>C (ATRIP) MANE Select NP_569055.1:n.*1103T>C
NM_001271023.2:c.*1103T>C (ATRIP) NP_001257952.1:n.*1103T>C
NM_007248.5:c.-18-11T>C (TREX1) NP_009179.2:n.-18-11T>C
NM_032166.4:c.*1103T>C (ATRIP) NP_115542.2:n.*1103T>C
NM_001271022.2:c.*1103T>C (ATRIP) NP_001257951.1:n.*1103T>C