Canonical Allele Identifier: CA2577942518
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513687_142513690dup , CM000665.2:g.142513687_142513690dup GRCh38
NC_000003.11:g.142232529_142232532dup , CM000665.1:g.142232529_142232532dup GRCh37
NC_000003.10:g.143715219_143715222dup NCBI36
NG_008951.1:g.70138_70141dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.4504-51_4504-48dup MANE Select ENSP00000343741.4:n.4504-51_4504-48dup
ENST00000653868.1:n.4533-51_4533-48dup
ENST00000656590.1:c.3294-51_3294-48dup
ENST00000661310.1:c.4312-51_4312-48dup ENSP00000499589.1:n.4312-51_4312-48dup
ENST00000350721.8:c.4504-51_4504-48dup ENSP00000343741.4:n.4504-51_4504-48dup
NM_001184.3:c.4504-51_4504-48dup NP_001175.2:n.4504-51_4504-48dup
XM_011512924.1:c.4510-51_4510-48dup XP_011511226.1:n.4510-51_4510-48dup
XM_011512925.1:c.4318-51_4318-48dup XP_011511227.1:n.4318-51_4318-48dup
XM_011512926.1:c.4510-51_4510-48dup XP_011511228.1:n.4510-51_4510-48dup
XM_011512927.1:c.4510-51_4510-48dup XP_011511229.1:n.4510-51_4510-48dup
XR_924147.1:n.4599-51_4599-48dup
XR_924148.1:n.4599-51_4599-48dup
XR_924149.1:n.4599-51_4599-48dup
NM_001354579.1:c.4312-51_4312-48dup NP_001341508.1:n.4312-51_4312-48dup
XR_001740179.2:n.4593-51_4593-48dup
XR_001740180.2:n.4599-51_4599-48dup
XR_001740181.2:n.4599-51_4599-48dup
XR_001740182.1:n.4599-51_4599-48dup
XR_002959543.1:n.4599-51_4599-48dup
XR_924148.2:n.4599-51_4599-48dup
NM_001184.4:c.4504-51_4504-48dup MANE Select NP_001175.2:n.4504-51_4504-48dup
NM_001354579.2:c.4312-51_4312-48dup NP_001341508.1:n.4312-51_4312-48dup