Canonical Allele Identifier: CA2586973091
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513634_142513642dup , CM000665.2:g.142513634_142513642dup GRCh38
NC_000003.11:g.142232476_142232484dup , CM000665.1:g.142232476_142232484dup GRCh37
NC_000003.10:g.143715166_143715174dup NCBI36
NG_008951.1:g.70188_70196dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.4504-1_4511dup
ENST00000653868.1:n.4533-1_4540dup
ENST00000656590.1:c.3294-1_3301dup
ENST00000661310.1:c.4312-1_4319dup
ENST00000350721.8:c.4504-1_4511dup
NM_001184.3:c.4504-1_4511dup
XM_011512924.1:c.4510-1_4517dup
XM_011512925.1:c.4318-1_4325dup
XM_011512926.1:c.4510-1_4517dup
XM_011512927.1:c.4510-1_4517dup
XR_924147.1:n.4599-1_4606dup
XR_924148.1:n.4599-1_4606dup
XR_924149.1:n.4599-1_4606dup
NM_001354579.1:c.4312-1_4319dup
XR_001740179.2:n.4593-1_4600dup
XR_001740180.2:n.4599-1_4606dup
XR_001740181.2:n.4599-1_4606dup
XR_001740182.1:n.4599-1_4606dup
XR_002959543.1:n.4599-1_4606dup
XR_924148.2:n.4599-1_4606dup
NM_001184.4:c.4504-1_4511dup
NM_001354579.2:c.4312-1_4319dup