Canonical Allele Identifier: CA1363031013

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466812C= , CM000665.2:g.48466812C= GRCh38
NC_000003.11:g.48508211C= , CM000665.1:g.48508211C= GRCh37
NC_000003.10:g.48483215C= NCBI36
NG_009820.1:g.5983C=
NG_033100.1:g.39049G=
NG_041782.1:g.25103C=
NG_009820.2:g.5983C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1258C= (ATRIP) MANE Select ENSP00000323099.3:n.*1258C=
ENST00000492235.2:c.-261C= (TREX1) ENSP00000494511.1:n.-261C=
ENST00000625293.3:c.157C= (TREX1) MANE Select ENSP00000486676.2:p.Pro53=
ENST00000634384.2:c.2752C= (ATRIP)
ENST00000635452.2:c.-261C= (TREX1) ENSP00000492023.2:n.-261C=
ENST00000296443.11:c.157C= ENSP00000296443.11:p.Pro53=
ENST00000433541.1:c.-261C= (TREX1) ENSP00000412404.1:n.-261C=
ENST00000444177.1:c.127C= (TREX1) ENSP00000415972.1:p.Pro43=
ENST00000456089.1:c.-8-253C= (TREX1) ENSP00000411331.1:n.-8-253C=
ENST00000492235.1:n.75C= (TREX1)
ENST00000625293.1:c.322C= (TREX1) ENSP00000486676.1:p.Pro108=
ENST00000629913.1:c.157C= (TREX1) ENSP00000486444.1:p.Pro53=
ENST00000634384.1:c.*2977C= ENSP00000489041.1:n.*2977C=
ENST00000635452.1:n.1364C=
ENST00000635464.1:c.3110C= ENSP00000489199.1:n.3110C=
NM_007248.3:c.127C= (TREX1) NP_009179.2:p.Pro43=
NM_016381.5:c.322C= (TREX1) NP_057465.1:p.Pro108=
NM_033629.4:c.157C= (TREX1) NP_338599.1:p.Pro53=
NM_007248.4:c.127C= (TREX1) NP_009179.2:p.Pro43=
NM_033629.5:c.157C= (TREX1) NP_338599.1:p.Pro53=
NR_153405.1:n.3466C=
NM_033629.6:c.157C= (TREX1) MANE Select NP_338599.1:p.Pro53=
NM_130384.3:c.*1258C= (ATRIP) MANE Select NP_569055.1:n.*1258C=
NM_001271023.2:c.*1258C= (ATRIP) NP_001257952.1:n.*1258C=
NM_007248.5:c.127C= (TREX1) NP_009179.2:p.Pro43=
NM_032166.4:c.*1258C= (ATRIP) NP_115542.2:n.*1258C=
NM_001271022.2:c.*1258C= (ATRIP) NP_001257951.1:n.*1258C=