Canonical Allele Identifier: CA1363030965

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466719A= , CM000665.2:g.48466719A= GRCh38
NC_000003.11:g.48508118A= , CM000665.1:g.48508118A= GRCh37
NC_000003.10:g.48483122A= NCBI36
NG_009820.1:g.5890A=
NG_033100.1:g.39142T=
NG_041782.1:g.25010A=
NG_009820.2:g.5890A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1165A= (ATRIP) MANE Select ENSP00000323099.3:n.*1165A=
ENST00000492235.2:c.-295-59A= (TREX1) ENSP00000494511.1:n.-295-59A=
ENST00000625293.3:c.64A= (TREX1) MANE Select ENSP00000486676.2:p.Thr22=
ENST00000634384.2:c.2659A= (ATRIP)
ENST00000635452.2:c.-333-21A= (TREX1) ENSP00000492023.2:n.-333-21A=
ENST00000296443.11:c.64A= ENSP00000296443.11:p.Thr22=
ENST00000433541.1:c.-333-21A= (TREX1) ENSP00000412404.1:n.-333-21A=
ENST00000444177.1:c.34A= (TREX1) ENSP00000415972.1:p.Thr12=
ENST00000456089.1:c.-8-346A= (TREX1) ENSP00000411331.1:n.-8-346A=
ENST00000492235.1:n.41-59A= (TREX1)
ENST00000625293.1:c.229A= (TREX1) ENSP00000486676.1:p.Thr77=
ENST00000629913.1:c.64A= (TREX1) ENSP00000486444.1:p.Thr22=
ENST00000634384.1:c.*2884A= ENSP00000489041.1:n.*2884A=
ENST00000635452.1:n.1271A=
ENST00000635464.1:c.3017A= ENSP00000489199.1:n.3017A=
NM_007248.3:c.34A= (TREX1) NP_009179.2:p.Thr12=
NM_016381.5:c.229A= (TREX1) NP_057465.1:p.Thr77=
NM_033629.4:c.64A= (TREX1) NP_338599.1:p.Thr22=
NM_007248.4:c.34A= (TREX1) NP_009179.2:p.Thr12=
NM_033629.5:c.64A= (TREX1) NP_338599.1:p.Thr22=
NR_153405.1:n.3373A=
NM_033629.6:c.64A= (TREX1) MANE Select NP_338599.1:p.Thr22=
NM_130384.3:c.*1165A= (ATRIP) MANE Select NP_569055.1:n.*1165A=
NM_001271023.2:c.*1165A= (ATRIP) NP_001257952.1:n.*1165A=
NM_007248.5:c.34A= (TREX1) NP_009179.2:p.Thr12=
NM_032166.4:c.*1165A= (ATRIP) NP_115542.2:n.*1165A=
NM_001271022.2:c.*1165A= (ATRIP) NP_001257951.1:n.*1165A=