Canonical Allele Identifier: CA1407011145
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513764_142513765delinsAT , CM000665.2:g.142513764_142513765delinsAT GRCh38
NC_000003.11:g.142232606_142232607delinsAT , CM000665.1:g.142232606_142232607delinsAT GRCh37
NC_000003.10:g.143715296_143715297delinsAT NCBI36
NG_008951.1:g.70062_70063delinsAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.4504-127_4504-126delinsAT MANE Select ENSP00000343741.4:n.4504-127_4504-126delinsAT
ENST00000653868.1:n.4533-127_4533-126delinsAT
ENST00000656590.1:c.3294-127_3294-126delinsAT
ENST00000661310.1:c.4312-127_4312-126delinsAT ENSP00000499589.1:n.4312-127_4312-126delinsAT
ENST00000350721.8:c.4504-127_4504-126delinsAT ENSP00000343741.4:n.4504-127_4504-126delinsAT
NM_001184.3:c.4504-127_4504-126delinsAT NP_001175.2:n.4504-127_4504-126delinsAT
XM_011512924.1:c.4510-127_4510-126delinsAT XP_011511226.1:n.4510-127_4510-126delinsAT
XM_011512925.1:c.4318-127_4318-126delinsAT XP_011511227.1:n.4318-127_4318-126delinsAT
XM_011512926.1:c.4510-127_4510-126delinsAT XP_011511228.1:n.4510-127_4510-126delinsAT
XM_011512927.1:c.4510-127_4510-126delinsAT XP_011511229.1:n.4510-127_4510-126delinsAT
XR_924147.1:n.4599-127_4599-126delinsAT
XR_924148.1:n.4599-127_4599-126delinsAT
XR_924149.1:n.4599-127_4599-126delinsAT
NM_001354579.1:c.4312-127_4312-126delinsAT NP_001341508.1:n.4312-127_4312-126delinsAT
XR_001740179.2:n.4593-127_4593-126delinsAT
XR_001740180.2:n.4599-127_4599-126delinsAT
XR_001740181.2:n.4599-127_4599-126delinsAT
XR_001740182.1:n.4599-127_4599-126delinsAT
XR_002959543.1:n.4599-127_4599-126delinsAT
XR_924148.2:n.4599-127_4599-126delinsAT
NM_001184.4:c.4504-127_4504-126delinsAT MANE Select NP_001175.2:n.4504-127_4504-126delinsAT
NM_001354579.2:c.4312-127_4312-126delinsAT NP_001341508.1:n.4312-127_4312-126delinsAT