Canonical Allele Identifier: CA2376771

Gene: ATRIP TREX1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467637T>C , CM000665.2:g.48467637T>C	GRCh38
NC_000003.11:g.48509036T>C , CM000665.1:g.48509036T>C	GRCh37
NC_000003.10:g.48484040T>C	NCBI36
NG_009820.1:g.6808T>C
NG_033100.1:g.38224A>G
NG_041782.1:g.25928T>C
NG_009820.2:g.6808T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*2083T>C (ATRIP) MANE Select	ENSP00000323099.3:n.*2083T>C
ENST00000492235.2:c.*37T>C (TREX1)	ENSP00000494511.1:n.*37T>C
ENST00000625293.3:c.*37T>C (TREX1) MANE Select	ENSP00000486676.2:n.*37T>C
ENST00000634384.2:c.3577T>C (ATRIP)
ENST00000635452.2:c.*37T>C (TREX1)	ENSP00000492023.2:n.*37T>C
ENST00000296443.11:c.*37T>C	ENSP00000296443.11:n.*37T>C
ENST00000433541.1:c.*37T>C (TREX1)	ENSP00000412404.1:n.*37T>C
ENST00000444177.1:c.*37T>C (TREX1)	ENSP00000415972.1:n.*37T>C
ENST00000456089.1:c.*37T>C (TREX1)	ENSP00000411331.1:n.*37T>C
ENST00000625293.1:c.*37T>C (TREX1)	ENSP00000486676.1:n.*37T>C
ENST00000634384.1:c.*3802T>C	ENSP00000489041.1:n.*3802T>C
ENST00000635452.1:n.2189T>C
ENST00000635464.1:c.3935T>C	ENSP00000489199.1:n.3935T>C
NM_007248.3:c.*37T>C (TREX1)	NP_009179.2:n.*37T>C
NM_016381.5:c.*37T>C (TREX1)	NP_057465.1:n.*37T>C
NM_033629.4:c.*37T>C (TREX1)	NP_338599.1:n.*37T>C
NM_007248.4:c.*37T>C (TREX1)	NP_009179.2:n.*37T>C
NM_033629.5:c.*37T>C (TREX1)	NP_338599.1:n.*37T>C
NR_153405.1:n.4291T>C
NM_033629.6:c.*37T>C (TREX1) MANE Select	NP_338599.1:n.*37T>C
NM_130384.3:c.*2083T>C (ATRIP) MANE Select	NP_569055.1:n.*2083T>C
NM_001271023.2:c.*2083T>C (ATRIP)	NP_001257952.1:n.*2083T>C
NM_007248.5:c.*37T>C (TREX1)	NP_009179.2:n.*37T>C
NM_032166.4:c.*2083T>C (ATRIP)	NP_115542.2:n.*2083T>C
NM_001271022.2:c.*2083T>C (ATRIP)	NP_001257951.1:n.*2083T>C