Canonical Allele Identifier: CA352618833

Gene: ATRIP TREX1

Linked Data

• gnomAD v4: 3-48467296-C-T
• MyVariant Identifiers: chr3:g.48508695C>T (hg19) ; chr3:g.48467296C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467296C>T , CM000665.2:g.48467296C>T	GRCh38
NC_000003.11:g.48508695C>T , CM000665.1:g.48508695C>T	GRCh37
NC_000003.10:g.48483699C>T	NCBI36
NG_009820.1:g.6467C>T
NG_033100.1:g.38565G>A
NG_041782.1:g.25587C>T
NG_009820.2:g.6467C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*1742C>T (ATRIP) MANE Select	ENSP00000323099.3:n.*1742C>T
ENST00000492235.2:c.224C>T (TREX1)	ENSP00000494511.1:p.Ala75Val
ENST00000625293.3:c.641C>T (TREX1) MANE Select	ENSP00000486676.2:p.Ala214Val
ENST00000634384.2:c.3236C>T (ATRIP)
ENST00000635452.2:c.224C>T (TREX1)	ENSP00000492023.2:p.Ala75Val
ENST00000296443.11:c.641C>T	ENSP00000296443.11:p.Ala214Val
ENST00000433541.1:c.224C>T (TREX1)	ENSP00000412404.1:p.Ala75Val
ENST00000444177.1:c.611C>T (TREX1)	ENSP00000415972.1:p.Ala204Val
ENST00000456089.1:c.224C>T (TREX1)	ENSP00000411331.1:p.Ala75Val
ENST00000492235.1:n.559C>T (TREX1)
ENST00000625293.1:c.806C>T (TREX1)	ENSP00000486676.1:p.Ala269Val
ENST00000629913.1:c.641C>T (TREX1)	ENSP00000486444.1:p.Ala214Val
ENST00000634384.1:c.*3461C>T	ENSP00000489041.1:n.*3461C>T
ENST00000635452.1:n.1848C>T
ENST00000635464.1:c.3594C>T	ENSP00000489199.1:n.3594C>T
NM_007248.3:c.611C>T (TREX1)	NP_009179.2:p.Ala204Val
NM_016381.5:c.806C>T (TREX1)	NP_057465.1:p.Ala269Val
NM_033629.4:c.641C>T (TREX1)	NP_338599.1:p.Ala214Val
NM_007248.4:c.611C>T (TREX1)	NP_009179.2:p.Ala204Val
NM_033629.5:c.641C>T (TREX1)	NP_338599.1:p.Ala214Val
NR_153405.1:n.3950C>T
NM_033629.6:c.641C>T (TREX1) MANE Select	NP_338599.1:p.Ala214Val
NM_130384.3:c.*1742C>T (ATRIP) MANE Select	NP_569055.1:n.*1742C>T
NM_001271023.2:c.*1742C>T (ATRIP)	NP_001257952.1:n.*1742C>T
NM_007248.5:c.611C>T (TREX1)	NP_009179.2:p.Ala204Val
NM_032166.4:c.*1742C>T (ATRIP)	NP_115542.2:n.*1742C>T
NM_001271022.2:c.*1742C>T (ATRIP)	NP_001257951.1:n.*1742C>T