Canonical Allele Identifier: CA352616692

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466627C>G , CM000665.2:g.48466627C>G GRCh38
NC_000003.11:g.48508026C>G , CM000665.1:g.48508026C>G GRCh37
NC_000003.10:g.48483030C>G NCBI36
NG_009820.1:g.5798C>G
NG_033100.1:g.39234G>C
NG_041782.1:g.24918C>G
NG_009820.2:g.5798C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1073C>G (ATRIP) MANE Select ENSP00000323099.3:n.*1073C>G
ENST00000492235.2:c.-295-151C>G (TREX1) ENSP00000494511.1:n.-295-151C>G
ENST00000625293.3:c.-26-3C>G (TREX1) MANE Select ENSP00000486676.2:n.-26-3C>G
ENST00000634384.2:c.2570-3C>G (ATRIP)
ENST00000635452.2:c.-333-113C>G (TREX1) ENSP00000492023.2:n.-333-113C>G
ENST00000296443.11:c.-26-3C>G ENSP00000296443.11:n.-26-3C>G
ENST00000433541.1:c.-345-3C>G (TREX1) ENSP00000412404.1:n.-345-3C>G
ENST00000444177.1:c.-18-41C>G (TREX1) ENSP00000415972.1:n.-18-41C>G
ENST00000456089.1:c.-9+318C>G (TREX1) ENSP00000411331.1:n.-9+318C>G
ENST00000492235.1:n.41-151C>G (TREX1)
ENST00000625293.1:c.137C>G (TREX1) ENSP00000486676.1:p.Pro46Arg
ENST00000629913.1:c.-26-3C>G (TREX1) ENSP00000486444.1:n.-26-3C>G
ENST00000634384.1:c.*2795-3C>G ENSP00000489041.1:n.*2795-3C>G
ENST00000635452.1:n.1179C>G
ENST00000635464.1:c.2928-3C>G ENSP00000489199.1:n.2928-3C>G
NM_007248.3:c.-18-41C>G (TREX1) NP_009179.2:n.-18-41C>G
NM_016381.5:c.137C>G (TREX1) NP_057465.1:p.Pro46Arg
NM_033629.4:c.-26-3C>G (TREX1) NP_338599.1:n.-26-3C>G
NM_007248.4:c.-18-41C>G (TREX1) NP_009179.2:n.-18-41C>G
NM_033629.5:c.-26-3C>G (TREX1) NP_338599.1:n.-26-3C>G
NR_153405.1:n.3284-3C>G
NM_033629.6:c.-26-3C>G (TREX1) MANE Select NP_338599.1:n.-26-3C>G
NM_130384.3:c.*1073C>G (ATRIP) MANE Select NP_569055.1:n.*1073C>G
NM_001271023.2:c.*1073C>G (ATRIP) NP_001257952.1:n.*1073C>G
NM_007248.5:c.-18-41C>G (TREX1) NP_009179.2:n.-18-41C>G
NM_032166.4:c.*1073C>G (ATRIP) NP_115542.2:n.*1073C>G
NM_001271022.2:c.*1073C>G (ATRIP) NP_001257951.1:n.*1073C>G