Canonical Allele Identifier: CA2665603387

Linked Data

gnomAD v4: 3-48467605-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467605A>C , CM000665.2:g.48467605A>C GRCh38
NC_000003.11:g.48509004A>C , CM000665.1:g.48509004A>C GRCh37
NC_000003.10:g.48484008A>C NCBI36
NG_009820.1:g.6776A>C
NG_033100.1:g.38256T>G
NG_041782.1:g.25896A>C
NG_009820.2:g.6776A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*2051A>C (ATRIP) MANE Select ENSP00000323099.3:n.*2051A>C
ENST00000492235.2:c.*5A>C (TREX1) ENSP00000494511.1:n.*5A>C
ENST00000625293.3:c.*5A>C (TREX1) MANE Select ENSP00000486676.2:n.*5A>C
ENST00000634384.2:c.3545A>C (ATRIP)
ENST00000635452.2:c.*5A>C (TREX1) ENSP00000492023.2:n.*5A>C
ENST00000296443.11:c.*5A>C ENSP00000296443.11:n.*5A>C
ENST00000433541.1:c.*5A>C (TREX1) ENSP00000412404.1:n.*5A>C
ENST00000444177.1:c.*5A>C (TREX1) ENSP00000415972.1:n.*5A>C
ENST00000456089.1:c.*5A>C (TREX1) ENSP00000411331.1:n.*5A>C
ENST00000625293.1:c.*5A>C (TREX1) ENSP00000486676.1:n.*5A>C
ENST00000634384.1:c.*3770A>C ENSP00000489041.1:n.*3770A>C
ENST00000635452.1:n.2157A>C
ENST00000635464.1:c.3903A>C ENSP00000489199.1:n.3903A>C
NM_007248.3:c.*5A>C (TREX1) NP_009179.2:n.*5A>C
NM_016381.5:c.*5A>C (TREX1) NP_057465.1:n.*5A>C
NM_033629.4:c.*5A>C (TREX1) NP_338599.1:n.*5A>C
NM_007248.4:c.*5A>C (TREX1) NP_009179.2:n.*5A>C
NM_033629.5:c.*5A>C (TREX1) NP_338599.1:n.*5A>C
NR_153405.1:n.4259A>C
NM_033629.6:c.*5A>C (TREX1) MANE Select NP_338599.1:n.*5A>C
NM_130384.3:c.*2051A>C (ATRIP) MANE Select NP_569055.1:n.*2051A>C
NM_001271023.2:c.*2051A>C (ATRIP) NP_001257952.1:n.*2051A>C
NM_007248.5:c.*5A>C (TREX1) NP_009179.2:n.*5A>C
NM_032166.4:c.*2051A>C (ATRIP) NP_115542.2:n.*2051A>C
NM_001271022.2:c.*2051A>C (ATRIP) NP_001257951.1:n.*2051A>C