Canonical Allele Identifier: CA354805752
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470131T>G , CM000665.2:g.142470131T>G GRCh38
NC_000003.11:g.142188973T>G , CM000665.1:g.142188973T>G GRCh37
NC_000003.10:g.143671663T>G NCBI36
NG_008951.1:g.113696A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6274A>C MANE Select ENSP00000343741.4:p.Thr2092Pro
ENST00000513291.2:n.1458A>C
ENST00000654170.1:n.1117A>C
ENST00000656590.1:c.5064A>C
ENST00000661310.1:c.6082A>C ENSP00000499589.1:p.Thr2028Pro
ENST00000665483.1:n.129A>C
ENST00000666447.1:n.109A>C
ENST00000666943.1:n.1738A>C
ENST00000350721.8:c.6274A>C ENSP00000343741.4:p.Thr2092Pro
NM_001184.3:c.6274A>C NP_001175.2:p.Thr2092Pro
XM_011512924.1:c.6280A>C XP_011511226.1:p.Thr2094Pro
XM_011512925.1:c.6088A>C XP_011511227.1:p.Thr2030Pro
XR_924147.1:n.6369A>C
XR_924148.1:n.6369A>C
XR_924149.1:n.6248A>C
NM_001354579.1:c.6082A>C NP_001341508.1:p.Thr2028Pro
XR_001740179.2:n.6363A>C
XR_001740180.2:n.6417A>C
XR_001740181.2:n.6296A>C
XR_001740182.1:n.6248A>C
XR_002959543.1:n.6473A>C
XR_924148.2:n.6369A>C
NM_001184.4:c.6274A>C MANE Select NP_001175.2:p.Thr2092Pro
NM_001354579.2:c.6082A>C NP_001341508.1:p.Thr2028Pro