Canonical Allele Identifier: CA2559915383
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553768_142553771del , CM000665.2:g.142553768_142553771del GRCh38
NC_000003.11:g.142272610_142272613del , CM000665.1:g.142272610_142272613del GRCh37
NC_000003.10:g.143755300_143755303del NCBI36
NG_008951.1:g.30059_30062del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2533-28_2533-25del MANE Select ENSP00000343741.4:n.2533-28_2533-25del
ENST00000515149.3:c.*1307-28_*1307-25del ENSP00000425897.3:n.*1307-28_*1307-25del
ENST00000653868.1:n.2562-28_2562-25del
ENST00000656590.1:c.1323-28_1323-25del
ENST00000659195.1:n.5408-28_5408-25del
ENST00000661310.1:c.2341-28_2341-25del ENSP00000499589.1:n.2341-28_2341-25del
ENST00000350721.8:c.2533-28_2533-25del ENSP00000343741.4:n.2533-28_2533-25del
NM_001184.3:c.2533-28_2533-25del NP_001175.2:n.2533-28_2533-25del
XM_011512924.1:c.2533-28_2533-25del XP_011511226.1:n.2533-28_2533-25del
XM_011512925.1:c.2341-28_2341-25del XP_011511227.1:n.2341-28_2341-25del
XM_011512926.1:c.2533-28_2533-25del XP_011511228.1:n.2533-28_2533-25del
XM_011512927.1:c.2533-28_2533-25del XP_011511229.1:n.2533-28_2533-25del
XR_924147.1:n.2622-28_2622-25del
XR_924148.1:n.2622-28_2622-25del
XR_924149.1:n.2622-28_2622-25del
NM_001354579.1:c.2341-28_2341-25del NP_001341508.1:n.2341-28_2341-25del
XR_001740179.2:n.2622-28_2622-25del
XR_001740180.2:n.2622-28_2622-25del
XR_001740181.2:n.2622-28_2622-25del
XR_001740182.1:n.2622-28_2622-25del
XR_002959543.1:n.2622-28_2622-25del
XR_924148.2:n.2622-28_2622-25del
NM_001184.4:c.2533-28_2533-25del MANE Select NP_001175.2:n.2533-28_2533-25del
NM_001354579.2:c.2341-28_2341-25del NP_001341508.1:n.2341-28_2341-25del