Canonical Allele Identifier: CA433616420

Linked Data

ClinVar Variation Id: 2947989
ClinVar RCV Id: RCV003806811
dbSNP Id: rs2040392001
MyVariant Identifiers: chr3:g.48508972A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467573A>G , CM000665.2:g.48467573A>G GRCh38
NC_000003.11:g.48508972A>G , CM000665.1:g.48508972A>G GRCh37
NC_000003.10:g.48483976A>G NCBI36
NG_009820.1:g.6744A>G
NG_033100.1:g.38288T>C
NG_041782.1:g.25864A>G
NG_009820.2:g.6744A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*2019A>G (ATRIP) MANE Select ENSP00000323099.3:n.*2019A>G
ENST00000492235.2:c.501A>G (TREX1) ENSP00000494511.1:p.Gly167=
ENST00000625293.3:c.918A>G (TREX1) MANE Select ENSP00000486676.2:p.Gly306=
ENST00000634384.2:c.3513A>G (ATRIP)
ENST00000635452.2:c.501A>G (TREX1) ENSP00000492023.2:p.Gly167=
ENST00000296443.11:c.918A>G ENSP00000296443.11:p.Gly306=
ENST00000433541.1:c.501A>G (TREX1) ENSP00000412404.1:p.Gly167=
ENST00000444177.1:c.888A>G (TREX1) ENSP00000415972.1:p.Gly296=
ENST00000456089.1:c.501A>G (TREX1) ENSP00000411331.1:p.Gly167=
ENST00000625293.1:c.1083A>G (TREX1) ENSP00000486676.1:p.Gly361=
ENST00000629913.1:c.918A>G (TREX1) ENSP00000486444.1:p.Gly306=
ENST00000634384.1:c.*3738A>G ENSP00000489041.1:n.*3738A>G
ENST00000635452.1:n.2125A>G
ENST00000635464.1:c.3871A>G ENSP00000489199.1:n.3871A>G
NM_007248.3:c.888A>G (TREX1) NP_009179.2:p.Gly296=
NM_016381.5:c.1083A>G (TREX1) NP_057465.1:p.Gly361=
NM_033629.4:c.918A>G (TREX1) NP_338599.1:p.Gly306=
NM_007248.4:c.888A>G (TREX1) NP_009179.2:p.Gly296=
NM_033629.5:c.918A>G (TREX1) NP_338599.1:p.Gly306=
NR_153405.1:n.4227A>G
NM_033629.6:c.918A>G (TREX1) MANE Select NP_338599.1:p.Gly306=
NM_130384.3:c.*2019A>G (ATRIP) MANE Select NP_569055.1:n.*2019A>G
NM_001271023.2:c.*2019A>G (ATRIP) NP_001257952.1:n.*2019A>G
NM_007248.5:c.888A>G (TREX1) NP_009179.2:p.Gly296=
NM_032166.4:c.*2019A>G (ATRIP) NP_115542.2:n.*2019A>G
NM_001271022.2:c.*2019A>G (ATRIP) NP_001257951.1:n.*2019A>G