Canonical Allele Identifier: CA352620249

Linked Data

gnomAD v4: 3-48467557-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.48467557T>G , CM000665.2:g.48467557T>G GRCh38
NC_000003.11:g.48508956T>G , CM000665.1:g.48508956T>G GRCh37
NC_000003.10:g.48483960T>G NCBI36
NG_009820.1:g.6728T>G
NG_033100.1:g.38304A>C
NG_041782.1:g.25848T>G
NG_009820.2:g.6728T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000320211.10:c.*2003T>G (ATRIP) MANE Select ENSP00000323099.3:n.*2003T>G
ENST00000492235.2:c.485T>G (TREX1) ENSP00000494511.1:p.Val162Gly
ENST00000625293.3:c.902T>G (TREX1) MANE Select ENSP00000486676.2:p.Val301Gly
ENST00000634384.2:c.3497T>G (ATRIP)
ENST00000635452.2:c.485T>G (TREX1) ENSP00000492023.2:p.Val162Gly
ENST00000296443.11:c.902T>G ENSP00000296443.11:p.Val301Gly
ENST00000433541.1:c.485T>G (TREX1) ENSP00000412404.1:p.Val162Gly
ENST00000444177.1:c.872T>G (TREX1) ENSP00000415972.1:p.Val291Gly
ENST00000456089.1:c.485T>G (TREX1) ENSP00000411331.1:p.Val162Gly
ENST00000625293.1:c.1067T>G (TREX1) ENSP00000486676.1:p.Val356Gly
ENST00000629913.1:c.902T>G (TREX1) ENSP00000486444.1:p.Val301Gly
ENST00000634384.1:c.*3722T>G ENSP00000489041.1:n.*3722T>G
ENST00000635452.1:n.2109T>G
ENST00000635464.1:c.3855T>G ENSP00000489199.1:n.3855T>G
NM_007248.3:c.872T>G (TREX1) NP_009179.2:p.Val291Gly
NM_016381.5:c.1067T>G (TREX1) NP_057465.1:p.Val356Gly
NM_033629.4:c.902T>G (TREX1) NP_338599.1:p.Val301Gly
NM_007248.4:c.872T>G (TREX1) NP_009179.2:p.Val291Gly
NM_033629.5:c.902T>G (TREX1) NP_338599.1:p.Val301Gly
NR_153405.1:n.4211T>G
NM_033629.6:c.902T>G (TREX1) MANE Select NP_338599.1:p.Val301Gly
NM_130384.3:c.*2003T>G (ATRIP) MANE Select NP_569055.1:n.*2003T>G
NM_001271023.2:c.*2003T>G (ATRIP) NP_001257952.1:n.*2003T>G
NM_007248.5:c.872T>G (TREX1) NP_009179.2:p.Val291Gly
NM_032166.4:c.*2003T>G (ATRIP) NP_115542.2:n.*2003T>G
NM_001271022.2:c.*2003T>G (ATRIP) NP_001257951.1:n.*2003T>G