Canonical Allele Identifier: CA1406991880
Gene: ATR HGNC NCBI

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6265C= MANE Select ENSP00000343741.4:p.Arg2089=
ENST00000513291.2:n.1449C=
ENST00000654170.1:n.1108C=
ENST00000656590.1:c.5055C=
ENST00000661310.1:c.6073C= ENSP00000499589.1:p.Arg2025=
ENST00000665483.1:n.120C=
ENST00000666447.1:n.100C=
ENST00000666943.1:n.1729C=
ENST00000350721.8:c.6265C= ENSP00000343741.4:p.Arg2089=
NM_001184.3:c.6265C= NP_001175.2:p.Arg2089=
XM_011512924.1:c.6271C= XP_011511226.1:p.Arg2091=
XM_011512925.1:c.6079C= XP_011511227.1:p.Arg2027=
XR_924147.1:n.6360C=
XR_924148.1:n.6360C=
XR_924149.1:n.6239C=
NM_001354579.1:c.6073C= NP_001341508.1:p.Arg2025=
XR_001740179.2:n.6354C=
XR_001740180.2:n.6408C=
XR_001740181.2:n.6287C=
XR_001740182.1:n.6239C=
XR_002959543.1:n.6464C=
XR_924148.2:n.6360C=
NM_001184.4:c.6265C= MANE Select NP_001175.2:p.Arg2089=
NM_001354579.2:c.6073C= NP_001341508.1:p.Arg2025=