Canonical Allele Identifier: CA352617055

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466720C>G , CM000665.2:g.48466720C>G GRCh38
NC_000003.11:g.48508119C>G , CM000665.1:g.48508119C>G GRCh37
NC_000003.10:g.48483123C>G NCBI36
NG_009820.1:g.5891C>G
NG_033100.1:g.39141G>C
NG_041782.1:g.25011C>G
NG_009820.2:g.5891C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1166C>G (ATRIP) MANE Select ENSP00000323099.3:n.*1166C>G
ENST00000492235.2:c.-295-58C>G (TREX1) ENSP00000494511.1:n.-295-58C>G
ENST00000625293.3:c.65C>G (TREX1) MANE Select ENSP00000486676.2:p.Thr22Ser
ENST00000634384.2:c.2660C>G (ATRIP)
ENST00000635452.2:c.-333-20C>G (TREX1) ENSP00000492023.2:n.-333-20C>G
ENST00000296443.11:c.65C>G ENSP00000296443.11:p.Thr22Ser
ENST00000433541.1:c.-333-20C>G (TREX1) ENSP00000412404.1:n.-333-20C>G
ENST00000444177.1:c.35C>G (TREX1) ENSP00000415972.1:p.Thr12Ser
ENST00000456089.1:c.-8-345C>G (TREX1) ENSP00000411331.1:n.-8-345C>G
ENST00000492235.1:n.41-58C>G (TREX1)
ENST00000625293.1:c.230C>G (TREX1) ENSP00000486676.1:p.Thr77Ser
ENST00000629913.1:c.65C>G (TREX1) ENSP00000486444.1:p.Thr22Ser
ENST00000634384.1:c.*2885C>G ENSP00000489041.1:n.*2885C>G
ENST00000635452.1:n.1272C>G
ENST00000635464.1:c.3018C>G ENSP00000489199.1:n.3018C>G
NM_007248.3:c.35C>G (TREX1) NP_009179.2:p.Thr12Ser
NM_016381.5:c.230C>G (TREX1) NP_057465.1:p.Thr77Ser
NM_033629.4:c.65C>G (TREX1) NP_338599.1:p.Thr22Ser
NM_007248.4:c.35C>G (TREX1) NP_009179.2:p.Thr12Ser
NM_033629.5:c.65C>G (TREX1) NP_338599.1:p.Thr22Ser
NR_153405.1:n.3374C>G
NM_033629.6:c.65C>G (TREX1) MANE Select NP_338599.1:p.Thr22Ser
NM_130384.3:c.*1166C>G (ATRIP) MANE Select NP_569055.1:n.*1166C>G
NM_001271023.2:c.*1166C>G (ATRIP) NP_001257952.1:n.*1166C>G
NM_007248.5:c.35C>G (TREX1) NP_009179.2:p.Thr12Ser
NM_032166.4:c.*1166C>G (ATRIP) NP_115542.2:n.*1166C>G
NM_001271022.2:c.*1166C>G (ATRIP) NP_001257951.1:n.*1166C>G