Canonical Allele Identifier: CA433616352

Linked Data

MyVariant Identifiers: chr3:g.48508723C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467324C>G , CM000665.2:g.48467324C>G GRCh38
NC_000003.11:g.48508723C>G , CM000665.1:g.48508723C>G GRCh37
NC_000003.10:g.48483727C>G NCBI36
NG_009820.1:g.6495C>G
NG_033100.1:g.38537G>C
NG_041782.1:g.25615C>G
NG_009820.2:g.6495C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1770C>G (ATRIP) MANE Select ENSP00000323099.3:n.*1770C>G
ENST00000492235.2:c.252C>G (TREX1) ENSP00000494511.1:p.Ala84=
ENST00000625293.3:c.669C>G (TREX1) MANE Select ENSP00000486676.2:p.Ala223=
ENST00000634384.2:c.3264C>G (ATRIP)
ENST00000635452.2:c.252C>G (TREX1) ENSP00000492023.2:p.Ala84=
ENST00000296443.11:c.669C>G ENSP00000296443.11:p.Ala223=
ENST00000433541.1:c.252C>G (TREX1) ENSP00000412404.1:p.Ala84=
ENST00000444177.1:c.639C>G (TREX1) ENSP00000415972.1:p.Ala213=
ENST00000456089.1:c.252C>G (TREX1) ENSP00000411331.1:p.Ala84=
ENST00000492235.1:n.587C>G (TREX1)
ENST00000625293.1:c.834C>G (TREX1) ENSP00000486676.1:p.Ala278=
ENST00000629913.1:c.669C>G (TREX1) ENSP00000486444.1:p.Ala223=
ENST00000634384.1:c.*3489C>G ENSP00000489041.1:n.*3489C>G
ENST00000635452.1:n.1876C>G
ENST00000635464.1:c.3622C>G ENSP00000489199.1:n.3622C>G
NM_007248.3:c.639C>G (TREX1) NP_009179.2:p.Ala213=
NM_016381.5:c.834C>G (TREX1) NP_057465.1:p.Ala278=
NM_033629.4:c.669C>G (TREX1) NP_338599.1:p.Ala223=
NM_007248.4:c.639C>G (TREX1) NP_009179.2:p.Ala213=
NM_033629.5:c.669C>G (TREX1) NP_338599.1:p.Ala223=
NR_153405.1:n.3978C>G
NM_033629.6:c.669C>G (TREX1) MANE Select NP_338599.1:p.Ala223=
NM_130384.3:c.*1770C>G (ATRIP) MANE Select NP_569055.1:n.*1770C>G
NM_001271023.2:c.*1770C>G (ATRIP) NP_001257952.1:n.*1770C>G
NM_007248.5:c.639C>G (TREX1) NP_009179.2:p.Ala213=
NM_032166.4:c.*1770C>G (ATRIP) NP_115542.2:n.*1770C>G
NM_001271022.2:c.*1770C>G (ATRIP) NP_001257951.1:n.*1770C>G