Canonical Allele Identifier: CA433615788

Linked Data

MyVariant Identifiers: chr3:g.48508546A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467147A>C , CM000665.2:g.48467147A>C GRCh38
NC_000003.11:g.48508546A>C , CM000665.1:g.48508546A>C GRCh37
NC_000003.10:g.48483550A>C NCBI36
NG_009820.1:g.6318A>C
NG_033100.1:g.38714T>G
NG_041782.1:g.25438A>C
NG_009820.2:g.6318A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000320211.10:c.*1593A>C (ATRIP) MANE Select ENSP00000323099.3:n.*1593A>C
ENST00000492235.2:c.75A>C (TREX1) ENSP00000494511.1:p.Arg25=
ENST00000625293.3:c.492A>C (TREX1) MANE Select ENSP00000486676.2:p.Arg164=
ENST00000634384.2:c.3087A>C (ATRIP)
ENST00000635452.2:c.75A>C (TREX1) ENSP00000492023.2:p.Arg25=
ENST00000296443.11:c.492A>C ENSP00000296443.11:p.Arg164=
ENST00000433541.1:c.75A>C (TREX1) ENSP00000412404.1:p.Arg25=
ENST00000444177.1:c.462A>C (TREX1) ENSP00000415972.1:p.Arg154=
ENST00000456089.1:c.75A>C (TREX1) ENSP00000411331.1:p.Arg25=
ENST00000492235.1:n.410A>C (TREX1)
ENST00000625293.1:c.657A>C (TREX1) ENSP00000486676.1:p.Arg219=
ENST00000629913.1:c.492A>C (TREX1) ENSP00000486444.1:p.Arg164=
ENST00000634384.1:c.*3312A>C ENSP00000489041.1:n.*3312A>C
ENST00000635452.1:n.1699A>C
ENST00000635464.1:c.3445A>C ENSP00000489199.1:n.3445A>C
NM_007248.3:c.462A>C (TREX1) NP_009179.2:p.Arg154=
NM_016381.5:c.657A>C (TREX1) NP_057465.1:p.Arg219=
NM_033629.4:c.492A>C (TREX1) NP_338599.1:p.Arg164=
NM_007248.4:c.462A>C (TREX1) NP_009179.2:p.Arg154=
NM_033629.5:c.492A>C (TREX1) NP_338599.1:p.Arg164=
NR_153405.1:n.3801A>C
NM_033629.6:c.492A>C (TREX1) MANE Select NP_338599.1:p.Arg164=
NM_130384.3:c.*1593A>C (ATRIP) MANE Select NP_569055.1:n.*1593A>C
NM_001271023.2:c.*1593A>C (ATRIP) NP_001257952.1:n.*1593A>C
NM_007248.5:c.462A>C (TREX1) NP_009179.2:p.Arg154=
NM_032166.4:c.*1593A>C (ATRIP) NP_115542.2:n.*1593A>C
NM_001271022.2:c.*1593A>C (ATRIP) NP_001257951.1:n.*1593A>C