Canonical Allele Identifier: CA1406991837

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470012_142470013delinsTG , CM000665.2:g.142470012_142470013delinsTG	GRCh38
NC_000003.11:g.142188854_142188855delinsTG , CM000665.1:g.142188854_142188855delinsTG	GRCh37
NC_000003.10:g.143671544_143671545delinsTG	NCBI36
NG_008951.1:g.113814_113815delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+73_6319+74delinsCA MANE Select	ENSP00000343741.4:n.6319+73_6319+74delins...
ENST00000513291.2:n.1503+73_1503+74delinsCA
ENST00000654170.1:n.1162+73_1162+74delinsCA
ENST00000656590.1:c.5109+73_5109+74delinsCA
ENST00000661310.1:c.6127+73_6127+74delinsCA	ENSP00000499589.1:n.6127+73_6127+74delins...
ENST00000665483.1:n.174+73_174+74delinsCA
ENST00000666447.1:n.154+73_154+74delinsCA
ENST00000666943.1:n.1783+73_1783+74delinsCA
ENST00000350721.8:c.6319+73_6319+74delinsCA	ENSP00000343741.4:n.6319+73_6319+74delins...
NM_001184.3:c.6319+73_6319+74delinsCA	NP_001175.2:n.6319+73_6319+74delinsCA
XM_011512924.1:c.6325+73_6325+74delinsCA	XP_011511226.1:n.6325+73_6325+74delinsCA
XM_011512925.1:c.6133+73_6133+74delinsCA	XP_011511227.1:n.6133+73_6133+74delinsCA
XR_924147.1:n.6414+73_6414+74delinsCA
XR_924148.1:n.6414+73_6414+74delinsCA
XR_924149.1:n.6293+73_6293+74delinsCA
NM_001354579.1:c.6127+73_6127+74delinsCA	NP_001341508.1:n.6127+73_6127+74delinsCA
XR_001740179.2:n.6408+73_6408+74delinsCA
XR_001740180.2:n.6462+73_6462+74delinsCA
XR_001740181.2:n.6341+73_6341+74delinsCA
XR_001740182.1:n.6293+73_6293+74delinsCA
XR_002959543.1:n.6518+73_6518+74delinsCA
XR_924148.2:n.6414+73_6414+74delinsCA
NM_001184.4:c.6319+73_6319+74delinsCA MANE Select	NP_001175.2:n.6319+73_6319+74delinsCA
NM_001354579.2:c.6127+73_6127+74delinsCA	NP_001341508.1:n.6127+73_6127+74delinsCA