Canonical Allele Identifier: CA352620348

Gene: ATRIP TREX1

Linked Data

• MyVariant Identifiers: chr3:g.48508980T>G (hg19) ; chr3:g.48467581T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467581T>G , CM000665.2:g.48467581T>G	GRCh38
NC_000003.11:g.48508980T>G , CM000665.1:g.48508980T>G	GRCh37
NC_000003.10:g.48483984T>G	NCBI36
NG_009820.1:g.6752T>G
NG_033100.1:g.38280A>C
NG_041782.1:g.25872T>G
NG_009820.2:g.6752T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*2027T>G (ATRIP) MANE Select	ENSP00000323099.3:n.*2027T>G
ENST00000492235.2:c.509T>G (TREX1)	ENSP00000494511.1:p.Leu170Arg
ENST00000625293.3:c.926T>G (TREX1) MANE Select	ENSP00000486676.2:p.Leu309Arg
ENST00000634384.2:c.3521T>G (ATRIP)
ENST00000635452.2:c.509T>G (TREX1)	ENSP00000492023.2:p.Leu170Arg
ENST00000296443.11:c.926T>G	ENSP00000296443.11:p.Leu309Arg
ENST00000433541.1:c.509T>G (TREX1)	ENSP00000412404.1:p.Leu170Arg
ENST00000444177.1:c.896T>G (TREX1)	ENSP00000415972.1:p.Leu299Arg
ENST00000456089.1:c.509T>G (TREX1)	ENSP00000411331.1:p.Leu170Arg
ENST00000625293.1:c.1091T>G (TREX1)	ENSP00000486676.1:p.Leu364Arg
ENST00000629913.1:c.926T>G (TREX1)	ENSP00000486444.1:p.Leu309Arg
ENST00000634384.1:c.*3746T>G	ENSP00000489041.1:n.*3746T>G
ENST00000635452.1:n.2133T>G
ENST00000635464.1:c.3879T>G	ENSP00000489199.1:n.3879T>G
NM_007248.3:c.896T>G (TREX1)	NP_009179.2:p.Leu299Arg
NM_016381.5:c.1091T>G (TREX1)	NP_057465.1:p.Leu364Arg
NM_033629.4:c.926T>G (TREX1)	NP_338599.1:p.Leu309Arg
NM_007248.4:c.896T>G (TREX1)	NP_009179.2:p.Leu299Arg
NM_033629.5:c.926T>G (TREX1)	NP_338599.1:p.Leu309Arg
NR_153405.1:n.4235T>G
NM_033629.6:c.926T>G (TREX1) MANE Select	NP_338599.1:p.Leu309Arg
NM_130384.3:c.*2027T>G (ATRIP) MANE Select	NP_569055.1:n.*2027T>G
NM_001271023.2:c.*2027T>G (ATRIP)	NP_001257952.1:n.*2027T>G
NM_007248.5:c.896T>G (TREX1)	NP_009179.2:p.Leu299Arg
NM_032166.4:c.*2027T>G (ATRIP)	NP_115542.2:n.*2027T>G
NM_001271022.2:c.*2027T>G (ATRIP)	NP_001257951.1:n.*2027T>G