Canonical Allele Identifier: CA433615604

Linked Data

MyVariant Identifiers: chr3:g.48508123C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48466724C>G , CM000665.2:g.48466724C>G GRCh38
NC_000003.11:g.48508123C>G , CM000665.1:g.48508123C>G GRCh37
NC_000003.10:g.48483127C>G NCBI36
NG_009820.1:g.5895C>G
NG_033100.1:g.39137G>C
NG_041782.1:g.25015C>G
NG_009820.2:g.5895C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1170C>G (ATRIP) MANE Select ENSP00000323099.3:n.*1170C>G
ENST00000492235.2:c.-295-54C>G (TREX1) ENSP00000494511.1:n.-295-54C>G
ENST00000625293.3:c.69C>G (TREX1) MANE Select ENSP00000486676.2:p.Gly23=
ENST00000634384.2:c.2664C>G (ATRIP)
ENST00000635452.2:c.-333-16C>G (TREX1) ENSP00000492023.2:n.-333-16C>G
ENST00000296443.11:c.69C>G ENSP00000296443.11:p.Gly23=
ENST00000433541.1:c.-333-16C>G (TREX1) ENSP00000412404.1:n.-333-16C>G
ENST00000444177.1:c.39C>G (TREX1) ENSP00000415972.1:p.Gly13=
ENST00000456089.1:c.-8-341C>G (TREX1) ENSP00000411331.1:n.-8-341C>G
ENST00000492235.1:n.41-54C>G (TREX1)
ENST00000625293.1:c.234C>G (TREX1) ENSP00000486676.1:p.Gly78=
ENST00000629913.1:c.69C>G (TREX1) ENSP00000486444.1:p.Gly23=
ENST00000634384.1:c.*2889C>G ENSP00000489041.1:n.*2889C>G
ENST00000635452.1:n.1276C>G
ENST00000635464.1:c.3022C>G ENSP00000489199.1:n.3022C>G
NM_007248.3:c.39C>G (TREX1) NP_009179.2:p.Gly13=
NM_016381.5:c.234C>G (TREX1) NP_057465.1:p.Gly78=
NM_033629.4:c.69C>G (TREX1) NP_338599.1:p.Gly23=
NM_007248.4:c.39C>G (TREX1) NP_009179.2:p.Gly13=
NM_033629.5:c.69C>G (TREX1) NP_338599.1:p.Gly23=
NR_153405.1:n.3378C>G
NM_033629.6:c.69C>G (TREX1) MANE Select NP_338599.1:p.Gly23=
NM_130384.3:c.*1170C>G (ATRIP) MANE Select NP_569055.1:n.*1170C>G
NM_001271023.2:c.*1170C>G (ATRIP) NP_001257952.1:n.*1170C>G
NM_007248.5:c.39C>G (TREX1) NP_009179.2:p.Gly13=
NM_032166.4:c.*1170C>G (ATRIP) NP_115542.2:n.*1170C>G
NM_001271022.2:c.*1170C>G (ATRIP) NP_001257951.1:n.*1170C>G