Canonical Allele Identifier: CA543045056

Gene: ATRIP TREX1

Linked Data

• dbSNP Id: rs1371605173
• gnomAD v2: 3-48509040-C-T
• gnomAD v3: 3-48467641-C-T
• gnomAD v4: 3-48467641-C-T
• MyVariant Identifiers: chr3:g.48509040C>T (hg19) ; chr3:g.48467641C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467641C>T , CM000665.2:g.48467641C>T	GRCh38
NC_000003.11:g.48509040C>T , CM000665.1:g.48509040C>T	GRCh37
NC_000003.10:g.48484044C>T	NCBI36
NG_009820.1:g.6812C>T
NG_033100.1:g.38220G>A
NG_041782.1:g.25932C>T
NG_009820.2:g.6812C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*2087C>T (ATRIP) MANE Select	ENSP00000323099.3:n.*2087C>T
ENST00000492235.2:c.*41C>T (TREX1)	ENSP00000494511.1:n.*41C>T
ENST00000625293.3:c.*41C>T (TREX1) MANE Select	ENSP00000486676.2:n.*41C>T
ENST00000634384.2:c.3581C>T (ATRIP)
ENST00000635452.2:c.*41C>T (TREX1)	ENSP00000492023.2:n.*41C>T
ENST00000296443.11:c.*41C>T	ENSP00000296443.11:n.*41C>T
ENST00000433541.1:c.*41C>T (TREX1)	ENSP00000412404.1:n.*41C>T
ENST00000444177.1:c.*41C>T (TREX1)	ENSP00000415972.1:n.*41C>T
ENST00000456089.1:c.*41C>T (TREX1)	ENSP00000411331.1:n.*41C>T
ENST00000625293.1:c.*41C>T (TREX1)	ENSP00000486676.1:n.*41C>T
ENST00000634384.1:c.*3806C>T	ENSP00000489041.1:n.*3806C>T
ENST00000635452.1:n.2193C>T
ENST00000635464.1:c.3939C>T	ENSP00000489199.1:n.3939C>T
NM_007248.3:c.*41C>T (TREX1)	NP_009179.2:n.*41C>T
NM_016381.5:c.*41C>T (TREX1)	NP_057465.1:n.*41C>T
NM_033629.4:c.*41C>T (TREX1)	NP_338599.1:n.*41C>T
NM_007248.4:c.*41C>T (TREX1)	NP_009179.2:n.*41C>T
NM_033629.5:c.*41C>T (TREX1)	NP_338599.1:n.*41C>T
NR_153405.1:n.4295C>T
NM_033629.6:c.*41C>T (TREX1) MANE Select	NP_338599.1:n.*41C>T
NM_130384.3:c.*2087C>T (ATRIP) MANE Select	NP_569055.1:n.*2087C>T
NM_001271023.2:c.*2087C>T (ATRIP)	NP_001257952.1:n.*2087C>T
NM_007248.5:c.*41C>T (TREX1)	NP_009179.2:n.*41C>T
NM_032166.4:c.*2087C>T (ATRIP)	NP_115542.2:n.*2087C>T
NM_001271022.2:c.*2087C>T (ATRIP)	NP_001257951.1:n.*2087C>T