Canonical Allele Identifier: CA352618021

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467050C>G , CM000665.2:g.48467050C>G GRCh38
NC_000003.11:g.48508449C>G , CM000665.1:g.48508449C>G GRCh37
NC_000003.10:g.48483453C>G NCBI36
NG_009820.1:g.6221C>G
NG_033100.1:g.38811G>C
NG_041782.1:g.25341C>G
NG_009820.2:g.6221C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1496C>G (ATRIP) MANE Select ENSP00000323099.3:n.*1496C>G
ENST00000492235.2:c.-23C>G (TREX1) ENSP00000494511.1:n.-23C>G
ENST00000625293.3:c.395C>G (TREX1) MANE Select ENSP00000486676.2:p.Pro132Arg
ENST00000634384.2:c.2990C>G (ATRIP)
ENST00000635452.2:c.-23C>G (TREX1) ENSP00000492023.2:n.-23C>G
ENST00000296443.11:c.395C>G ENSP00000296443.11:p.Pro132Arg
ENST00000433541.1:c.-23C>G (TREX1) ENSP00000412404.1:n.-23C>G
ENST00000444177.1:c.365C>G (TREX1) ENSP00000415972.1:p.Pro122Arg
ENST00000456089.1:c.-8-15C>G (TREX1) ENSP00000411331.1:n.-8-15C>G
ENST00000492235.1:n.313C>G (TREX1)
ENST00000625293.1:c.560C>G (TREX1) ENSP00000486676.1:p.Pro187Arg
ENST00000629913.1:c.395C>G (TREX1) ENSP00000486444.1:p.Pro132Arg
ENST00000634384.1:c.*3215C>G ENSP00000489041.1:n.*3215C>G
ENST00000635452.1:n.1602C>G
ENST00000635464.1:c.3348C>G ENSP00000489199.1:n.3348C>G
NM_007248.3:c.365C>G (TREX1) NP_009179.2:p.Pro122Arg
NM_016381.5:c.560C>G (TREX1) NP_057465.1:p.Pro187Arg
NM_033629.4:c.395C>G (TREX1) NP_338599.1:p.Pro132Arg
NM_007248.4:c.365C>G (TREX1) NP_009179.2:p.Pro122Arg
NM_033629.5:c.395C>G (TREX1) NP_338599.1:p.Pro132Arg
NR_153405.1:n.3704C>G
NM_033629.6:c.395C>G (TREX1) MANE Select NP_338599.1:p.Pro132Arg
NM_130384.3:c.*1496C>G (ATRIP) MANE Select NP_569055.1:n.*1496C>G
NM_001271023.2:c.*1496C>G (ATRIP) NP_001257952.1:n.*1496C>G
NM_007248.5:c.365C>G (TREX1) NP_009179.2:p.Pro122Arg
NM_032166.4:c.*1496C>G (ATRIP) NP_115542.2:n.*1496C>G
NM_001271022.2:c.*1496C>G (ATRIP) NP_001257951.1:n.*1496C>G