Canonical Allele Identifier: CA2376770

Linked Data

dbSNP Id: rs777007205
gnomAD v2: 3-48509034-G-A
gnomAD v4: 3-48467635-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467635G>A , CM000665.2:g.48467635G>A GRCh38
NC_000003.11:g.48509034G>A , CM000665.1:g.48509034G>A GRCh37
NC_000003.10:g.48484038G>A NCBI36
NG_009820.1:g.6806G>A
NG_033100.1:g.38226C>T
NG_041782.1:g.25926G>A
NG_009820.2:g.6806G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*2081G>A (ATRIP) MANE Select ENSP00000323099.3:n.*2081G>A
ENST00000492235.2:c.*35G>A (TREX1) ENSP00000494511.1:n.*35G>A
ENST00000625293.3:c.*35G>A (TREX1) MANE Select ENSP00000486676.2:n.*35G>A
ENST00000634384.2:c.3575G>A (ATRIP)
ENST00000635452.2:c.*35G>A (TREX1) ENSP00000492023.2:n.*35G>A
ENST00000296443.11:c.*35G>A ENSP00000296443.11:n.*35G>A
ENST00000433541.1:c.*35G>A (TREX1) ENSP00000412404.1:n.*35G>A
ENST00000444177.1:c.*35G>A (TREX1) ENSP00000415972.1:n.*35G>A
ENST00000456089.1:c.*35G>A (TREX1) ENSP00000411331.1:n.*35G>A
ENST00000625293.1:c.*35G>A (TREX1) ENSP00000486676.1:n.*35G>A
ENST00000634384.1:c.*3800G>A ENSP00000489041.1:n.*3800G>A
ENST00000635452.1:n.2187G>A
ENST00000635464.1:c.3933G>A ENSP00000489199.1:n.3933G>A
NM_007248.3:c.*35G>A (TREX1) NP_009179.2:n.*35G>A
NM_016381.5:c.*35G>A (TREX1) NP_057465.1:n.*35G>A
NM_033629.4:c.*35G>A (TREX1) NP_338599.1:n.*35G>A
NM_007248.4:c.*35G>A (TREX1) NP_009179.2:n.*35G>A
NM_033629.5:c.*35G>A (TREX1) NP_338599.1:n.*35G>A
NR_153405.1:n.4289G>A
NM_033629.6:c.*35G>A (TREX1) MANE Select NP_338599.1:n.*35G>A
NM_130384.3:c.*2081G>A (ATRIP) MANE Select NP_569055.1:n.*2081G>A
NM_001271023.2:c.*2081G>A (ATRIP) NP_001257952.1:n.*2081G>A
NM_007248.5:c.*35G>A (TREX1) NP_009179.2:n.*35G>A
NM_032166.4:c.*2081G>A (ATRIP) NP_115542.2:n.*2081G>A
NM_001271022.2:c.*2081G>A (ATRIP) NP_001257951.1:n.*2081G>A