Canonical Allele Identifier: CA2650302
Gene: ATR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs372271245

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553399C>T , CM000665.2:g.142553399C>T GRCh38
NC_000003.11:g.142272241C>T , CM000665.1:g.142272241C>T GRCh37
NC_000003.10:g.143754931C>T NCBI36
NG_008951.1:g.30428G>A

Transcript Alleles

HGVS Amino-acid change
NM_001184.3:c.2634-1G>A VV NP_001175.2:p.=
XM_011512924.1:c.2634-1G>A XP_011511226.1:p.=
XM_011512925.1:c.2442-1G>A XP_011511227.1:p.=
XM_011512926.1:c.2634-1G>A XP_011511228.1:p.=
XM_011512927.1:c.2634-1G>A XP_011511229.1:p.=
XR_924147.1:n.2723-1G>A
XR_924148.1:n.2723-1G>A
XR_924149.1:n.2723-1G>A
NM_001354579.1:c.2442-1G>A VV NP_001341508.1:p.=
XR_001740179.2:n.2723-1G>A
XR_001740180.2:n.2723-1G>A
XR_001740181.2:n.2723-1G>A
XR_001740182.1:n.2723-1G>A
XR_002959543.1:n.2723-1G>A
XR_924148.2:n.2723-1G>A
NM_001184.4:c.2634-1G>A VV MANE Preferred
ENST00000350721.8:c.2634-1G>A ENSP00000343741.4:p.=