Canonical Allele Identifier: CA354815780
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553721T>G , CM000665.2:g.142553721T>G GRCh38
NC_000003.11:g.142272563T>G , CM000665.1:g.142272563T>G GRCh37
NC_000003.10:g.143755253T>G NCBI36
NG_008951.1:g.30106A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2552A>C MANE Select ENSP00000343741.4:p.Lys851Thr
ENST00000515149.3:c.*1326A>C ENSP00000425897.3:n.*1326A>C
ENST00000653868.1:n.2581A>C
ENST00000656590.1:c.1342A>C
ENST00000659195.1:n.5427A>C
ENST00000661310.1:c.2360A>C ENSP00000499589.1:p.Lys787Thr
ENST00000350721.8:c.2552A>C ENSP00000343741.4:p.Lys851Thr
NM_001184.3:c.2552A>C NP_001175.2:p.Lys851Thr
XM_011512924.1:c.2552A>C XP_011511226.1:p.Lys851Thr
XM_011512925.1:c.2360A>C XP_011511227.1:p.Lys787Thr
XM_011512926.1:c.2552A>C XP_011511228.1:p.Lys851Thr
XM_011512927.1:c.2552A>C XP_011511229.1:p.Lys851Thr
XR_924147.1:n.2641A>C
XR_924148.1:n.2641A>C
XR_924149.1:n.2641A>C
NM_001354579.1:c.2360A>C NP_001341508.1:p.Lys787Thr
XR_001740179.2:n.2641A>C
XR_001740180.2:n.2641A>C
XR_001740181.2:n.2641A>C
XR_001740182.1:n.2641A>C
XR_002959543.1:n.2641A>C
XR_924148.2:n.2641A>C
NM_001184.4:c.2552A>C MANE Select NP_001175.2:p.Lys851Thr
NM_001354579.2:c.2360A>C NP_001341508.1:p.Lys787Thr