Canonical Allele Identifier: CA352618286

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467154A>G , CM000665.2:g.48467154A>G GRCh38
NC_000003.11:g.48508553A>G , CM000665.1:g.48508553A>G GRCh37
NC_000003.10:g.48483557A>G NCBI36
NG_009820.1:g.6325A>G
NG_033100.1:g.38707T>C
NG_041782.1:g.25445A>G
NG_009820.2:g.6325A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1600A>G (ATRIP) MANE Select ENSP00000323099.3:n.*1600A>G
ENST00000492235.2:c.82A>G (TREX1) ENSP00000494511.1:p.Ser28Gly
ENST00000625293.3:c.499A>G (TREX1) MANE Select ENSP00000486676.2:p.Ser167Gly
ENST00000634384.2:c.3094A>G (ATRIP)
ENST00000635452.2:c.82A>G (TREX1) ENSP00000492023.2:p.Ser28Gly
ENST00000296443.11:c.499A>G ENSP00000296443.11:p.Ser167Gly
ENST00000433541.1:c.82A>G (TREX1) ENSP00000412404.1:p.Ser28Gly
ENST00000444177.1:c.469A>G (TREX1) ENSP00000415972.1:p.Ser157Gly
ENST00000456089.1:c.82A>G (TREX1) ENSP00000411331.1:p.Ser28Gly
ENST00000492235.1:n.417A>G (TREX1)
ENST00000625293.1:c.664A>G (TREX1) ENSP00000486676.1:p.Ser222Gly
ENST00000629913.1:c.499A>G (TREX1) ENSP00000486444.1:p.Ser167Gly
ENST00000634384.1:c.*3319A>G ENSP00000489041.1:n.*3319A>G
ENST00000635452.1:n.1706A>G
ENST00000635464.1:c.3452A>G ENSP00000489199.1:n.3452A>G
NM_007248.3:c.469A>G (TREX1) NP_009179.2:p.Ser157Gly
NM_016381.5:c.664A>G (TREX1) NP_057465.1:p.Ser222Gly
NM_033629.4:c.499A>G (TREX1) NP_338599.1:p.Ser167Gly
NM_007248.4:c.469A>G (TREX1) NP_009179.2:p.Ser157Gly
NM_033629.5:c.499A>G (TREX1) NP_338599.1:p.Ser167Gly
NR_153405.1:n.3808A>G
NM_033629.6:c.499A>G (TREX1) MANE Select NP_338599.1:p.Ser167Gly
NM_130384.3:c.*1600A>G (ATRIP) MANE Select NP_569055.1:n.*1600A>G
NM_001271023.2:c.*1600A>G (ATRIP) NP_001257952.1:n.*1600A>G
NM_007248.5:c.469A>G (TREX1) NP_009179.2:p.Ser157Gly
NM_032166.4:c.*1600A>G (ATRIP) NP_115542.2:n.*1600A>G
NM_001271022.2:c.*1600A>G (ATRIP) NP_001257951.1:n.*1600A>G