Canonical Allele Identifier: CA2704304047

Gene: ATR

Linked Data

• dbSNP Id: rs2108375861

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513744_142513749del , CM000665.2:g.142513744_142513749del	GRCh38
NC_000003.11:g.142232586_142232591del , CM000665.1:g.142232586_142232591del	GRCh37
NC_000003.10:g.143715276_143715281del	NCBI36
NG_008951.1:g.70084_70089del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4504-105_4504-100del MANE Select	ENSP00000343741.4:n.4504-105_4504-100del
ENST00000653868.1:n.4533-105_4533-100del
ENST00000656590.1:c.3294-105_3294-100del
ENST00000661310.1:c.4312-105_4312-100del	ENSP00000499589.1:n.4312-105_4312-100del
ENST00000350721.8:c.4504-105_4504-100del	ENSP00000343741.4:n.4504-105_4504-100del
NM_001184.3:c.4504-105_4504-100del	NP_001175.2:n.4504-105_4504-100del
XM_011512924.1:c.4510-105_4510-100del	XP_011511226.1:n.4510-105_4510-100del
XM_011512925.1:c.4318-105_4318-100del	XP_011511227.1:n.4318-105_4318-100del
XM_011512926.1:c.4510-105_4510-100del	XP_011511228.1:n.4510-105_4510-100del
XM_011512927.1:c.4510-105_4510-100del	XP_011511229.1:n.4510-105_4510-100del
XR_924147.1:n.4599-105_4599-100del
XR_924148.1:n.4599-105_4599-100del
XR_924149.1:n.4599-105_4599-100del
NM_001354579.1:c.4312-105_4312-100del	NP_001341508.1:n.4312-105_4312-100del
XR_001740179.2:n.4593-105_4593-100del
XR_001740180.2:n.4599-105_4599-100del
XR_001740181.2:n.4599-105_4599-100del
XR_001740182.1:n.4599-105_4599-100del
XR_002959543.1:n.4599-105_4599-100del
XR_924148.2:n.4599-105_4599-100del
NM_001184.4:c.4504-105_4504-100del MANE Select	NP_001175.2:n.4504-105_4504-100del
NM_001354579.2:c.4312-105_4312-100del	NP_001341508.1:n.4312-105_4312-100del