Canonical Allele Identifier: CA352618669

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467253G>C , CM000665.2:g.48467253G>C GRCh38
NC_000003.11:g.48508652G>C , CM000665.1:g.48508652G>C GRCh37
NC_000003.10:g.48483656G>C NCBI36
NG_009820.1:g.6424G>C
NG_033100.1:g.38608C>G
NG_041782.1:g.25544G>C
NG_009820.2:g.6424G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320211.10:c.*1699G>C (ATRIP) MANE Select ENSP00000323099.3:n.*1699G>C
ENST00000492235.2:c.181G>C (TREX1) ENSP00000494511.1:p.Asp61His
ENST00000625293.3:c.598G>C (TREX1) MANE Select ENSP00000486676.2:p.Asp200His
ENST00000634384.2:c.3193G>C (ATRIP)
ENST00000635452.2:c.181G>C (TREX1) ENSP00000492023.2:p.Asp61His
ENST00000296443.11:c.598G>C ENSP00000296443.11:p.Asp200His
ENST00000433541.1:c.181G>C (TREX1) ENSP00000412404.1:p.Asp61His
ENST00000444177.1:c.568G>C (TREX1) ENSP00000415972.1:p.Asp190His
ENST00000456089.1:c.181G>C (TREX1) ENSP00000411331.1:p.Asp61His
ENST00000492235.1:n.516G>C (TREX1)
ENST00000625293.1:c.763G>C (TREX1) ENSP00000486676.1:p.Asp255His
ENST00000629913.1:c.598G>C (TREX1) ENSP00000486444.1:p.Asp200His
ENST00000634384.1:c.*3418G>C ENSP00000489041.1:n.*3418G>C
ENST00000635452.1:n.1805G>C
ENST00000635464.1:c.3551G>C ENSP00000489199.1:n.3551G>C
NM_007248.3:c.568G>C (TREX1) NP_009179.2:p.Asp190His
NM_016381.5:c.763G>C (TREX1) NP_057465.1:p.Asp255His
NM_033629.4:c.598G>C (TREX1) NP_338599.1:p.Asp200His
NM_007248.4:c.568G>C (TREX1) NP_009179.2:p.Asp190His
NM_033629.5:c.598G>C (TREX1) NP_338599.1:p.Asp200His
NR_153405.1:n.3907G>C
NM_033629.6:c.598G>C (TREX1) MANE Select NP_338599.1:p.Asp200His
NM_130384.3:c.*1699G>C (ATRIP) MANE Select NP_569055.1:n.*1699G>C
NM_001271023.2:c.*1699G>C (ATRIP) NP_001257952.1:n.*1699G>C
NM_007248.5:c.568G>C (TREX1) NP_009179.2:p.Asp190His
NM_032166.4:c.*1699G>C (ATRIP) NP_115542.2:n.*1699G>C
NM_001271022.2:c.*1699G>C (ATRIP) NP_001257951.1:n.*1699G>C