Canonical Allele Identifier: CA433615748

Linked Data

MyVariant Identifiers: chr3:g.48508738C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467339C>T , CM000665.2:g.48467339C>T GRCh38
NC_000003.11:g.48508738C>T , CM000665.1:g.48508738C>T GRCh37
NC_000003.10:g.48483742C>T NCBI36
NG_009820.1:g.6510C>T
NG_033100.1:g.38522G>A
NG_041782.1:g.25630C>T
NG_009820.2:g.6510C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*1785C>T (ATRIP) MANE Select ENSP00000323099.3:n.*1785C>T
ENST00000492235.2:c.267C>T (TREX1) ENSP00000494511.1:p.Thr89=
ENST00000625293.3:c.684C>T (TREX1) MANE Select ENSP00000486676.2:p.Thr228=
ENST00000634384.2:c.3279C>T (ATRIP)
ENST00000635452.2:c.267C>T (TREX1) ENSP00000492023.2:p.Thr89=
ENST00000296443.11:c.684C>T ENSP00000296443.11:p.Thr228=
ENST00000433541.1:c.267C>T (TREX1) ENSP00000412404.1:p.Thr89=
ENST00000444177.1:c.654C>T (TREX1) ENSP00000415972.1:p.Thr218=
ENST00000456089.1:c.267C>T (TREX1) ENSP00000411331.1:p.Thr89=
ENST00000492235.1:n.602C>T (TREX1)
ENST00000625293.1:c.849C>T (TREX1) ENSP00000486676.1:p.Thr283=
ENST00000629913.1:c.684C>T (TREX1) ENSP00000486444.1:p.Thr228=
ENST00000634384.1:c.*3504C>T ENSP00000489041.1:n.*3504C>T
ENST00000635452.1:n.1891C>T
ENST00000635464.1:c.3637C>T ENSP00000489199.1:n.3637C>T
NM_007248.3:c.654C>T (TREX1) NP_009179.2:p.Thr218=
NM_016381.5:c.849C>T (TREX1) NP_057465.1:p.Thr283=
NM_033629.4:c.684C>T (TREX1) NP_338599.1:p.Thr228=
NM_007248.4:c.654C>T (TREX1) NP_009179.2:p.Thr218=
NM_033629.5:c.684C>T (TREX1) NP_338599.1:p.Thr228=
NR_153405.1:n.3993C>T
NM_033629.6:c.684C>T (TREX1) MANE Select NP_338599.1:p.Thr228=
NM_130384.3:c.*1785C>T (ATRIP) MANE Select NP_569055.1:n.*1785C>T
NM_001271023.2:c.*1785C>T (ATRIP) NP_001257952.1:n.*1785C>T
NM_007248.5:c.654C>T (TREX1) NP_009179.2:p.Thr218=
NM_032166.4:c.*1785C>T (ATRIP) NP_115542.2:n.*1785C>T
NM_001271022.2:c.*1785C>T (ATRIP) NP_001257951.1:n.*1785C>T