Canonical Allele Identifier: CA2668041761
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513710_142513711del , CM000665.2:g.142513710_142513711del GRCh38
NC_000003.11:g.142232552_142232553del , CM000665.1:g.142232552_142232553del GRCh37
NC_000003.10:g.143715242_143715243del NCBI36
NG_008951.1:g.70118_70119del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.4504-71_4504-70del MANE Select ENSP00000343741.4:n.4504-71_4504-70del
ENST00000653868.1:n.4533-71_4533-70del
ENST00000656590.1:c.3294-71_3294-70del
ENST00000661310.1:c.4312-71_4312-70del ENSP00000499589.1:n.4312-71_4312-70del
ENST00000350721.8:c.4504-71_4504-70del ENSP00000343741.4:n.4504-71_4504-70del
NM_001184.3:c.4504-71_4504-70del NP_001175.2:n.4504-71_4504-70del
XM_011512924.1:c.4510-71_4510-70del XP_011511226.1:n.4510-71_4510-70del
XM_011512925.1:c.4318-71_4318-70del XP_011511227.1:n.4318-71_4318-70del
XM_011512926.1:c.4510-71_4510-70del XP_011511228.1:n.4510-71_4510-70del
XM_011512927.1:c.4510-71_4510-70del XP_011511229.1:n.4510-71_4510-70del
XR_924147.1:n.4599-71_4599-70del
XR_924148.1:n.4599-71_4599-70del
XR_924149.1:n.4599-71_4599-70del
NM_001354579.1:c.4312-71_4312-70del NP_001341508.1:n.4312-71_4312-70del
XR_001740179.2:n.4593-71_4593-70del
XR_001740180.2:n.4599-71_4599-70del
XR_001740181.2:n.4599-71_4599-70del
XR_001740182.1:n.4599-71_4599-70del
XR_002959543.1:n.4599-71_4599-70del
XR_924148.2:n.4599-71_4599-70del
NM_001184.4:c.4504-71_4504-70del MANE Select NP_001175.2:n.4504-71_4504-70del
NM_001354579.2:c.4312-71_4312-70del NP_001341508.1:n.4312-71_4312-70del