Canonical Allele Identifier: CA352620012

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467517C>G , CM000665.2:g.48467517C>G GRCh38
NC_000003.11:g.48508916C>G , CM000665.1:g.48508916C>G GRCh37
NC_000003.10:g.48483920C>G NCBI36
NG_009820.1:g.6688C>G
NG_033100.1:g.38344G>C
NG_041782.1:g.25808C>G
NG_009820.2:g.6688C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1963C>G (ATRIP) MANE Select ENSP00000323099.3:n.*1963C>G
ENST00000492235.2:c.445C>G (TREX1) ENSP00000494511.1:p.Leu149Val
ENST00000625293.3:c.862C>G (TREX1) MANE Select ENSP00000486676.2:p.Leu288Val
ENST00000634384.2:c.3457C>G (ATRIP)
ENST00000635452.2:c.445C>G (TREX1) ENSP00000492023.2:p.Leu149Val
ENST00000296443.11:c.862C>G ENSP00000296443.11:p.Leu288Val
ENST00000433541.1:c.445C>G (TREX1) ENSP00000412404.1:p.Leu149Val
ENST00000444177.1:c.832C>G (TREX1) ENSP00000415972.1:p.Leu278Val
ENST00000456089.1:c.445C>G (TREX1) ENSP00000411331.1:p.Leu149Val
ENST00000625293.1:c.1027C>G (TREX1) ENSP00000486676.1:p.Leu343Val
ENST00000629913.1:c.862C>G (TREX1) ENSP00000486444.1:p.Leu288Val
ENST00000634384.1:c.*3682C>G ENSP00000489041.1:n.*3682C>G
ENST00000635452.1:n.2069C>G
ENST00000635464.1:c.3815C>G ENSP00000489199.1:n.3815C>G
NM_007248.3:c.832C>G (TREX1) NP_009179.2:p.Leu278Val
NM_016381.5:c.1027C>G (TREX1) NP_057465.1:p.Leu343Val
NM_033629.4:c.862C>G (TREX1) NP_338599.1:p.Leu288Val
NM_007248.4:c.832C>G (TREX1) NP_009179.2:p.Leu278Val
NM_033629.5:c.862C>G (TREX1) NP_338599.1:p.Leu288Val
NR_153405.1:n.4171C>G
NM_033629.6:c.862C>G (TREX1) MANE Select NP_338599.1:p.Leu288Val
NM_130384.3:c.*1963C>G (ATRIP) MANE Select NP_569055.1:n.*1963C>G
NM_001271023.2:c.*1963C>G (ATRIP) NP_001257952.1:n.*1963C>G
NM_007248.5:c.832C>G (TREX1) NP_009179.2:p.Leu278Val
NM_032166.4:c.*1963C>G (ATRIP) NP_115542.2:n.*1963C>G
NM_001271022.2:c.*1963C>G (ATRIP) NP_001257951.1:n.*1963C>G