Canonical Allele Identifier: CA433615768

Gene: ATRIP TREX1

Linked Data

• MyVariant Identifiers: chr3:g.48508747C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.48467348C>T , CM000665.2:g.48467348C>T	GRCh38
NC_000003.11:g.48508747C>T , CM000665.1:g.48508747C>T	GRCh37
NC_000003.10:g.48483751C>T	NCBI36
NG_009820.1:g.6519C>T
NG_033100.1:g.38513G>A
NG_041782.1:g.25639C>T
NG_009820.2:g.6519C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000320211.10:c.*1794C>T (ATRIP) MANE Select	ENSP00000323099.3:n.*1794C>T
ENST00000492235.2:c.276C>T (TREX1)	ENSP00000494511.1:p.Pro92=
ENST00000625293.3:c.693C>T (TREX1) MANE Select	ENSP00000486676.2:p.Pro231=
ENST00000634384.2:c.3288C>T (ATRIP)
ENST00000635452.2:c.276C>T (TREX1)	ENSP00000492023.2:p.Pro92=
ENST00000296443.11:c.693C>T	ENSP00000296443.11:p.Pro231=
ENST00000433541.1:c.276C>T (TREX1)	ENSP00000412404.1:p.Pro92=
ENST00000444177.1:c.663C>T (TREX1)	ENSP00000415972.1:p.Pro221=
ENST00000456089.1:c.276C>T (TREX1)	ENSP00000411331.1:p.Pro92=
ENST00000492235.1:n.611C>T (TREX1)
ENST00000625293.1:c.858C>T (TREX1)	ENSP00000486676.1:p.Pro286=
ENST00000629913.1:c.693C>T (TREX1)	ENSP00000486444.1:p.Pro231=
ENST00000634384.1:c.*3513C>T	ENSP00000489041.1:n.*3513C>T
ENST00000635452.1:n.1900C>T
ENST00000635464.1:c.3646C>T	ENSP00000489199.1:n.3646C>T
NM_007248.3:c.663C>T (TREX1)	NP_009179.2:p.Pro221=
NM_016381.5:c.858C>T (TREX1)	NP_057465.1:p.Pro286=
NM_033629.4:c.693C>T (TREX1)	NP_338599.1:p.Pro231=
NM_007248.4:c.663C>T (TREX1)	NP_009179.2:p.Pro221=
NM_033629.5:c.693C>T (TREX1)	NP_338599.1:p.Pro231=
NR_153405.1:n.4002C>T
NM_033629.6:c.693C>T (TREX1) MANE Select	NP_338599.1:p.Pro231=
NM_130384.3:c.*1794C>T (ATRIP) MANE Select	NP_569055.1:n.*1794C>T
NM_001271023.2:c.*1794C>T (ATRIP)	NP_001257952.1:n.*1794C>T
NM_007248.5:c.663C>T (TREX1)	NP_009179.2:p.Pro221=
NM_032166.4:c.*1794C>T (ATRIP)	NP_115542.2:n.*1794C>T
NM_001271022.2:c.*1794C>T (ATRIP)	NP_001257951.1:n.*1794C>T