Canonical Allele Identifier: CA354805805
Gene: ATR HGNC NCBI

Linked Data

dbSNP Id: rs1158115459

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470140G>A , CM000665.2:g.142470140G>A GRCh38
NC_000003.11:g.142188982G>A , CM000665.1:g.142188982G>A GRCh37
NC_000003.10:g.143671672G>A NCBI36
NG_008951.1:g.113687C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6265C>T MANE Select ENSP00000343741.4:p.Arg2089Ter
ENST00000513291.2:n.1449C>T
ENST00000654170.1:n.1108C>T
ENST00000656590.1:c.5055C>T
ENST00000661310.1:c.6073C>T ENSP00000499589.1:p.Arg2025Ter
ENST00000665483.1:n.120C>T
ENST00000666447.1:n.100C>T
ENST00000666943.1:n.1729C>T
ENST00000350721.8:c.6265C>T ENSP00000343741.4:p.Arg2089Ter
NM_001184.3:c.6265C>T NP_001175.2:p.Arg2089Ter
XM_011512924.1:c.6271C>T XP_011511226.1:p.Arg2091Ter
XM_011512925.1:c.6079C>T XP_011511227.1:p.Arg2027Ter
XR_924147.1:n.6360C>T
XR_924148.1:n.6360C>T
XR_924149.1:n.6239C>T
NM_001354579.1:c.6073C>T NP_001341508.1:p.Arg2025Ter
XR_001740179.2:n.6354C>T
XR_001740180.2:n.6408C>T
XR_001740181.2:n.6287C>T
XR_001740182.1:n.6239C>T
XR_002959543.1:n.6464C>T
XR_924148.2:n.6360C>T
NM_001184.4:c.6265C>T MANE Select NP_001175.2:p.Arg2089Ter
NM_001354579.2:c.6073C>T NP_001341508.1:p.Arg2025Ter