Canonical Allele Identifier: CA899914363

Gene: ATR

Linked Data

• dbSNP Id: rs1280287438
• MyVariant Identifiers: chr3:g.142232764_142232765insAAAA (hg19) ; chr3:g.142513922_142513923insAAAA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513923_142513924insAAAA , CM000665.2:g.142513923_142513924insAAAA	GRCh38
NC_000003.11:g.142232765_142232766insAAAA , CM000665.1:g.142232765_142232766insAAAA	GRCh37
NC_000003.10:g.143715455_143715456insAAAA	NCBI36
NG_008951.1:g.69904_69905insTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4504-285_4504-284insTTTT MANE Select	ENSP00000343741.4:n.4504-285_4504-284insTTTT
ENST00000653868.1:n.4533-285_4533-284insTTTT
ENST00000656590.1:c.3294-285_3294-284insTTTT
ENST00000661310.1:c.4312-285_4312-284insTTTT	ENSP00000499589.1:n.4312-285_4312-284insTTTT
ENST00000350721.8:c.4504-285_4504-284insTTTT	ENSP00000343741.4:n.4504-285_4504-284insTTTT
NM_001184.3:c.4504-285_4504-284insTTTT	NP_001175.2:n.4504-285_4504-284insTTTT
XM_011512924.1:c.4510-285_4510-284insTTTT	XP_011511226.1:n.4510-285_4510-284insTTTT
XM_011512925.1:c.4318-285_4318-284insTTTT	XP_011511227.1:n.4318-285_4318-284insTTTT
XM_011512926.1:c.4510-285_4510-284insTTTT	XP_011511228.1:n.4510-285_4510-284insTTTT
XM_011512927.1:c.4510-285_4510-284insTTTT	XP_011511229.1:n.4510-285_4510-284insTTTT
XR_924147.1:n.4599-285_4599-284insTTTT
XR_924148.1:n.4599-285_4599-284insTTTT
XR_924149.1:n.4599-285_4599-284insTTTT
NM_001354579.1:c.4312-285_4312-284insTTTT	NP_001341508.1:n.4312-285_4312-284insTTTT
XR_001740179.2:n.4593-285_4593-284insTTTT
XR_001740180.2:n.4599-285_4599-284insTTTT
XR_001740181.2:n.4599-285_4599-284insTTTT
XR_001740182.1:n.4599-285_4599-284insTTTT
XR_002959543.1:n.4599-285_4599-284insTTTT
XR_924148.2:n.4599-285_4599-284insTTTT
NM_001184.4:c.4504-285_4504-284insTTTT MANE Select	NP_001175.2:n.4504-285_4504-284insTTTT
NM_001354579.2:c.4312-285_4312-284insTTTT	NP_001341508.1:n.4312-285_4312-284insTTTT