Canonical Allele Identifier: CA2376541
Community Standard Title: NM_033629.6(TREX1):c.1A>G (p.Met1Val)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466656A>G , CM000665.2:g.48466656A>G GRCh38
NC_000003.11:g.48508055A>G , CM000665.1:g.48508055A>G GRCh37
NC_000003.10:g.48483059A>G NCBI36
NG_009820.1:g.5827A>G
NG_033100.1:g.39205T>C
NG_041782.1:g.24947A>G
NG_009820.2:g.5827A>G

Transcript Alleles

HGVS Amino-acid Change
NM_033629.6:c.1A>G (TREX1) MANE Select NP_338599.1:p.Met1Val
NM_130384.3:c.*1102A>G (ATRIP) MANE Select NP_569055.1:n.*1102A>G
ENST00000320211.10:c.*1102A>G (ATRIP) MANE Select ENSP00000323099.3:n.*1102A>G
ENST00000625293.3:c.1A>G (TREX1) MANE Select ENSP00000486676.2:p.Met1Val
NM_001271022.2:c.*1102A>G (ATRIP) NP_001257951.1:n.*1102A>G
NM_001271023.2:c.*1102A>G (ATRIP) NP_001257952.1:n.*1102A>G
NM_007248.3:c.-18-12A>G (TREX1) NP_009179.2:n.-18-12A>G
NM_007248.4:c.-18-12A>G (TREX1) NP_009179.2:n.-18-12A>G
NM_007248.5:c.-18-12A>G (TREX1) NP_009179.2:n.-18-12A>G
NM_016381.5:c.166A>G (TREX1) NP_057465.1:p.Met56Val
NM_032166.4:c.*1102A>G (ATRIP) NP_115542.2:n.*1102A>G
NM_033629.4:c.1A>G (TREX1) NP_338599.1:p.Met1Val
NM_033629.5:c.1A>G (TREX1) NP_338599.1:p.Met1Val
NR_153405.1:n.3310A>G
ENST00000296443.11:c.1A>G ENSP00000296443.11:p.Met1Val
ENST00000433541.1:c.-334+15A>G (TREX1) ENSP00000412404.1:n.-334+15A>G
ENST00000444177.1:c.-18-12A>G (TREX1) ENSP00000415972.1:n.-18-12A>G
ENST00000456089.1:c.-9+347A>G (TREX1) ENSP00000411331.1:n.-9+347A>G
ENST00000492235.1:n.41-122A>G (TREX1)
ENST00000492235.2:c.-295-122A>G (TREX1) ENSP00000494511.1:n.-295-122A>G
ENST00000625293.1:c.166A>G (TREX1) ENSP00000486676.1:p.Met56Val
ENST00000629913.1:c.1A>G (TREX1) ENSP00000486444.1:p.Met1Val
ENST00000634384.1:c.*2821A>G ENSP00000489041.1:n.*2821A>G
ENST00000634384.2:c.2596A>G (ATRIP)
ENST00000635452.1:n.1208A>G
ENST00000635452.2:c.-333-84A>G (TREX1) ENSP00000492023.2:n.-333-84A>G
ENST00000635464.1:c.2954A>G ENSP00000489199.1:n.2954A>G