Canonical Allele Identifier: CA354805794
Gene: ATR HGNC NCBI

Linked Data

dbSNP Id: rs1270466103

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470136A>G , CM000665.2:g.142470136A>G GRCh38
NC_000003.11:g.142188978A>G , CM000665.1:g.142188978A>G GRCh37
NC_000003.10:g.143671668A>G NCBI36
NG_008951.1:g.113691T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6269T>C MANE Select ENSP00000343741.4:p.Met2090Thr
ENST00000513291.2:n.1453T>C
ENST00000654170.1:n.1112T>C
ENST00000656590.1:c.5059T>C
ENST00000661310.1:c.6077T>C ENSP00000499589.1:p.Met2026Thr
ENST00000665483.1:n.124T>C
ENST00000666447.1:n.104T>C
ENST00000666943.1:n.1733T>C
ENST00000350721.8:c.6269T>C ENSP00000343741.4:p.Met2090Thr
NM_001184.3:c.6269T>C NP_001175.2:p.Met2090Thr
XM_011512924.1:c.6275T>C XP_011511226.1:p.Met2092Thr
XM_011512925.1:c.6083T>C XP_011511227.1:p.Met2028Thr
XR_924147.1:n.6364T>C
XR_924148.1:n.6364T>C
XR_924149.1:n.6243T>C
NM_001354579.1:c.6077T>C NP_001341508.1:p.Met2026Thr
XR_001740179.2:n.6358T>C
XR_001740180.2:n.6412T>C
XR_001740181.2:n.6291T>C
XR_001740182.1:n.6243T>C
XR_002959543.1:n.6468T>C
XR_924148.2:n.6364T>C
NM_001184.4:c.6269T>C MANE Select NP_001175.2:p.Met2090Thr
NM_001354579.2:c.6077T>C NP_001341508.1:p.Met2026Thr