Canonical Allele Identifier: CA352620403

Gene: ATRIP TREX1

Linked Data

• MyVariant Identifiers: chr3:g.48508991G>T (hg19) ; chr3:g.48467592G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467592G>T , CM000665.2:g.48467592G>T	GRCh38
NC_000003.11:g.48508991G>T , CM000665.1:g.48508991G>T	GRCh37
NC_000003.10:g.48483995G>T	NCBI36
NG_009820.1:g.6763G>T
NG_033100.1:g.38269C>A
NG_041782.1:g.25883G>T
NG_009820.2:g.6763G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*2038G>T (ATRIP) MANE Select	ENSP00000323099.3:n.*2038G>T
ENST00000492235.2:c.520G>T (TREX1)	ENSP00000494511.1:p.Gly174Trp
ENST00000625293.3:c.937G>T (TREX1) MANE Select	ENSP00000486676.2:p.Gly313Trp
ENST00000634384.2:c.3532G>T (ATRIP)
ENST00000635452.2:c.520G>T (TREX1)	ENSP00000492023.2:p.Gly174Trp
ENST00000296443.11:c.937G>T	ENSP00000296443.11:p.Gly313Trp
ENST00000433541.1:c.520G>T (TREX1)	ENSP00000412404.1:p.Gly174Trp
ENST00000444177.1:c.907G>T (TREX1)	ENSP00000415972.1:p.Gly303Trp
ENST00000456089.1:c.520G>T (TREX1)	ENSP00000411331.1:p.Gly174Trp
ENST00000625293.1:c.1102G>T (TREX1)	ENSP00000486676.1:p.Gly368Trp
ENST00000629913.1:c.937G>T (TREX1)	ENSP00000486444.1:p.Gly313Trp
ENST00000634384.1:c.*3757G>T	ENSP00000489041.1:n.*3757G>T
ENST00000635452.1:n.2144G>T
ENST00000635464.1:c.3890G>T	ENSP00000489199.1:n.3890G>T
NM_007248.3:c.907G>T (TREX1)	NP_009179.2:p.Gly303Trp
NM_016381.5:c.1102G>T (TREX1)	NP_057465.1:p.Gly368Trp
NM_033629.4:c.937G>T (TREX1)	NP_338599.1:p.Gly313Trp
NM_007248.4:c.907G>T (TREX1)	NP_009179.2:p.Gly303Trp
NM_033629.5:c.937G>T (TREX1)	NP_338599.1:p.Gly313Trp
NR_153405.1:n.4246G>T
NM_033629.6:c.937G>T (TREX1) MANE Select	NP_338599.1:p.Gly313Trp
NM_130384.3:c.*2038G>T (ATRIP) MANE Select	NP_569055.1:n.*2038G>T
NM_001271023.2:c.*2038G>T (ATRIP)	NP_001257952.1:n.*2038G>T
NM_007248.5:c.907G>T (TREX1)	NP_009179.2:p.Gly303Trp
NM_032166.4:c.*2038G>T (ATRIP)	NP_115542.2:n.*2038G>T
NM_001271022.2:c.*2038G>T (ATRIP)	NP_001257951.1:n.*2038G>T