Canonical Allele Identifier: CA10654756

Linked Data

ClinVar Variation Id: 369666
ClinVar RCV Id: RCV000408633
dbSNP Id: rs184953805
gnomAD v4: 3-48467284-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467284G>A , CM000665.2:g.48467284G>A GRCh38
NC_000003.11:g.48508683G>A , CM000665.1:g.48508683G>A GRCh37
NC_000003.10:g.48483687G>A NCBI36
NG_009820.1:g.6455G>A
NG_033100.1:g.38577C>T
NG_041782.1:g.25575G>A
NG_009820.2:g.6455G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000320211.10:c.*1730G>A (ATRIP) MANE Select ENSP00000323099.3:n.*1730G>A
ENST00000492235.2:c.212G>A (TREX1) ENSP00000494511.1:p.Trp71Ter
ENST00000625293.3:c.629G>A (TREX1) MANE Select ENSP00000486676.2:p.Trp210Ter
ENST00000634384.2:c.3224G>A (ATRIP)
ENST00000635452.2:c.212G>A (TREX1) ENSP00000492023.2:p.Trp71Ter
ENST00000296443.11:c.629G>A ENSP00000296443.11:p.Trp210Ter
ENST00000433541.1:c.212G>A (TREX1) ENSP00000412404.1:p.Trp71Ter
ENST00000444177.1:c.599G>A (TREX1) ENSP00000415972.1:p.Trp200Ter
ENST00000456089.1:c.212G>A (TREX1) ENSP00000411331.1:p.Trp71Ter
ENST00000492235.1:n.547G>A (TREX1)
ENST00000625293.1:c.794G>A (TREX1) ENSP00000486676.1:p.Trp265Ter
ENST00000629913.1:c.629G>A (TREX1) ENSP00000486444.1:p.Trp210Ter
ENST00000634384.1:c.*3449G>A ENSP00000489041.1:n.*3449G>A
ENST00000635452.1:n.1836G>A
ENST00000635464.1:c.3582G>A ENSP00000489199.1:n.3582G>A
NM_007248.3:c.599G>A (TREX1) NP_009179.2:p.Trp200Ter
NM_016381.5:c.794G>A (TREX1) NP_057465.1:p.Trp265Ter
NM_033629.4:c.629G>A (TREX1) NP_338599.1:p.Trp210Ter
NM_007248.4:c.599G>A (TREX1) NP_009179.2:p.Trp200Ter
NM_033629.5:c.629G>A (TREX1) NP_338599.1:p.Trp210Ter
NR_153405.1:n.3938G>A
NM_033629.6:c.629G>A (TREX1) MANE Select NP_338599.1:p.Trp210Ter
NM_130384.3:c.*1730G>A (ATRIP) MANE Select NP_569055.1:n.*1730G>A
NM_001271023.2:c.*1730G>A (ATRIP) NP_001257952.1:n.*1730G>A
NM_007248.5:c.599G>A (TREX1) NP_009179.2:p.Trp200Ter
NM_032166.4:c.*1730G>A (ATRIP) NP_115542.2:n.*1730G>A
NM_001271022.2:c.*1730G>A (ATRIP) NP_001257951.1:n.*1730G>A