Canonical Allele Identifier: CA436125975
Gene: ATR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.142188980T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470138T>A , CM000665.2:g.142470138T>A GRCh38
NC_000003.11:g.142188980T>A , CM000665.1:g.142188980T>A GRCh37
NC_000003.10:g.143671670T>A NCBI36
NG_008951.1:g.113689A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6267A>T MANE Select ENSP00000343741.4:p.Arg2089=
ENST00000513291.2:n.1451A>T
ENST00000654170.1:n.1110A>T
ENST00000656590.1:c.5057A>T
ENST00000661310.1:c.6075A>T ENSP00000499589.1:p.Arg2025=
ENST00000665483.1:n.122A>T
ENST00000666447.1:n.102A>T
ENST00000666943.1:n.1731A>T
ENST00000350721.8:c.6267A>T ENSP00000343741.4:p.Arg2089=
NM_001184.3:c.6267A>T NP_001175.2:p.Arg2089=
XM_011512924.1:c.6273A>T XP_011511226.1:p.Arg2091=
XM_011512925.1:c.6081A>T XP_011511227.1:p.Arg2027=
XR_924147.1:n.6362A>T
XR_924148.1:n.6362A>T
XR_924149.1:n.6241A>T
NM_001354579.1:c.6075A>T NP_001341508.1:p.Arg2025=
XR_001740179.2:n.6356A>T
XR_001740180.2:n.6410A>T
XR_001740181.2:n.6289A>T
XR_001740182.1:n.6241A>T
XR_002959543.1:n.6466A>T
XR_924148.2:n.6362A>T
NM_001184.4:c.6267A>T MANE Select NP_001175.2:p.Arg2089=
NM_001354579.2:c.6075A>T NP_001341508.1:p.Arg2025=