Canonical Allele Identifier: CA2376701
Community Standard Title: NM_033629.6(TREX1):c.649C>T (p.Arg217Trp)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467304C>T , CM000665.2:g.48467304C>T GRCh38
NC_000003.11:g.48508703C>T , CM000665.1:g.48508703C>T GRCh37
NC_000003.10:g.48483707C>T NCBI36
NG_009820.1:g.6475C>T
NG_033100.1:g.38557G>A
NG_041782.1:g.25595C>T
NG_009820.2:g.6475C>T

Transcript Alleles

HGVS Amino-acid Change
NM_033629.6:c.649C>T (TREX1) MANE Select NP_338599.1:p.Arg217Trp
NM_130384.3:c.*1750C>T (ATRIP) MANE Select NP_569055.1:n.*1750C>T
ENST00000320211.10:c.*1750C>T (ATRIP) MANE Select ENSP00000323099.3:n.*1750C>T
ENST00000625293.3:c.649C>T (TREX1) MANE Select ENSP00000486676.2:p.Arg217Trp
NM_001271022.2:c.*1750C>T (ATRIP) NP_001257951.1:n.*1750C>T
NM_001271023.2:c.*1750C>T (ATRIP) NP_001257952.1:n.*1750C>T
NM_007248.3:c.619C>T (TREX1) NP_009179.2:p.Arg207Trp
NM_007248.4:c.619C>T (TREX1) NP_009179.2:p.Arg207Trp
NM_007248.5:c.619C>T (TREX1) NP_009179.2:p.Arg207Trp
NM_016381.5:c.814C>T (TREX1) NP_057465.1:p.Arg272Trp
NM_032166.4:c.*1750C>T (ATRIP) NP_115542.2:n.*1750C>T
NM_033629.4:c.649C>T (TREX1) NP_338599.1:p.Arg217Trp
NM_033629.5:c.649C>T (TREX1) NP_338599.1:p.Arg217Trp
NR_153405.1:n.3958C>T
ENST00000296443.11:c.649C>T ENSP00000296443.11:p.Arg217Trp
ENST00000433541.1:c.232C>T (TREX1) ENSP00000412404.1:p.Arg78Trp
ENST00000444177.1:c.619C>T (TREX1) ENSP00000415972.1:p.Arg207Trp
ENST00000456089.1:c.232C>T (TREX1) ENSP00000411331.1:p.Arg78Trp
ENST00000492235.1:n.567C>T (TREX1)
ENST00000492235.2:c.232C>T (TREX1) ENSP00000494511.1:p.Arg78Trp
ENST00000625293.1:c.814C>T (TREX1) ENSP00000486676.1:p.Arg272Trp
ENST00000629913.1:c.649C>T (TREX1) ENSP00000486444.1:p.Arg217Trp
ENST00000634384.1:c.*3469C>T ENSP00000489041.1:n.*3469C>T
ENST00000634384.2:c.3244C>T (ATRIP)
ENST00000635452.1:n.1856C>T
ENST00000635452.2:c.232C>T (TREX1) ENSP00000492023.2:p.Arg78Trp
ENST00000635464.1:c.3602C>T ENSP00000489199.1:n.3602C>T