Canonical Allele Identifier: CA2376601

Linked Data

ClinVar Variation Id: 522920
dbSNP Id: rs755919767
gnomAD v2: 3-48508272-C-T
gnomAD v3: 3-48466873-C-T
gnomAD v4: 3-48466873-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466873C>T , CM000665.2:g.48466873C>T GRCh38
NC_000003.11:g.48508272C>T , CM000665.1:g.48508272C>T GRCh37
NC_000003.10:g.48483276C>T NCBI36
NG_009820.1:g.6044C>T
NG_033100.1:g.38988G>A
NG_041782.1:g.25164C>T
NG_009820.2:g.6044C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1319C>T (ATRIP) MANE Select ENSP00000323099.3:n.*1319C>T
ENST00000492235.2:c.-200C>T (TREX1) ENSP00000494511.1:n.-200C>T
ENST00000625293.3:c.218C>T (TREX1) MANE Select ENSP00000486676.2:p.Pro73Leu
ENST00000634384.2:c.2813C>T (ATRIP)
ENST00000635452.2:c.-200C>T (TREX1) ENSP00000492023.2:n.-200C>T
ENST00000296443.11:c.218C>T ENSP00000296443.11:p.Pro73Leu
ENST00000433541.1:c.-200C>T (TREX1) ENSP00000412404.1:n.-200C>T
ENST00000444177.1:c.188C>T (TREX1) ENSP00000415972.1:p.Pro63Leu
ENST00000456089.1:c.-8-192C>T (TREX1) ENSP00000411331.1:n.-8-192C>T
ENST00000492235.1:n.136C>T (TREX1)
ENST00000625293.1:c.383C>T (TREX1) ENSP00000486676.1:p.Pro128Leu
ENST00000629913.1:c.218C>T (TREX1) ENSP00000486444.1:p.Pro73Leu
ENST00000634384.1:c.*3038C>T ENSP00000489041.1:n.*3038C>T
ENST00000635452.1:n.1425C>T
ENST00000635464.1:c.3171C>T ENSP00000489199.1:n.3171C>T
NM_007248.3:c.188C>T (TREX1) NP_009179.2:p.Pro63Leu
NM_016381.5:c.383C>T (TREX1) NP_057465.1:p.Pro128Leu
NM_033629.4:c.218C>T (TREX1) NP_338599.1:p.Pro73Leu
NM_007248.4:c.188C>T (TREX1) NP_009179.2:p.Pro63Leu
NM_033629.5:c.218C>T (TREX1) NP_338599.1:p.Pro73Leu
NR_153405.1:n.3527C>T
NM_033629.6:c.218C>T (TREX1) MANE Select NP_338599.1:p.Pro73Leu
NM_130384.3:c.*1319C>T (ATRIP) MANE Select NP_569055.1:n.*1319C>T
NM_001271023.2:c.*1319C>T (ATRIP) NP_001257952.1:n.*1319C>T
NM_007248.5:c.188C>T (TREX1) NP_009179.2:p.Pro63Leu
NM_032166.4:c.*1319C>T (ATRIP) NP_115542.2:n.*1319C>T
NM_001271022.2:c.*1319C>T (ATRIP) NP_001257951.1:n.*1319C>T