Canonical Allele Identifier: CA1406991834

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470002_142470003delinsGA , CM000665.2:g.142470002_142470003delinsGA	GRCh38
NC_000003.11:g.142188844_142188845delinsGA , CM000665.1:g.142188844_142188845delinsGA	GRCh37
NC_000003.10:g.143671534_143671535delinsGA	NCBI36
NG_008951.1:g.113824_113825delinsTC

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+83_6319+84delinsTC MANE Select	ENSP00000343741.4:n.6319+83_6319+84delins...
ENST00000513291.2:n.1503+83_1503+84delinsTC
ENST00000654170.1:n.1162+83_1162+84delinsTC
ENST00000656590.1:c.5109+83_5109+84delinsTC
ENST00000661310.1:c.6127+83_6127+84delinsTC	ENSP00000499589.1:n.6127+83_6127+84delins...
ENST00000665483.1:n.174+83_174+84delinsTC
ENST00000666447.1:n.154+83_154+84delinsTC
ENST00000666943.1:n.1783+83_1783+84delinsTC
ENST00000350721.8:c.6319+83_6319+84delinsTC	ENSP00000343741.4:n.6319+83_6319+84delins...
NM_001184.3:c.6319+83_6319+84delinsTC	NP_001175.2:n.6319+83_6319+84delinsTC
XM_011512924.1:c.6325+83_6325+84delinsTC	XP_011511226.1:n.6325+83_6325+84delinsTC
XM_011512925.1:c.6133+83_6133+84delinsTC	XP_011511227.1:n.6133+83_6133+84delinsTC
XR_924147.1:n.6414+83_6414+84delinsTC
XR_924148.1:n.6414+83_6414+84delinsTC
XR_924149.1:n.6293+83_6293+84delinsTC
NM_001354579.1:c.6127+83_6127+84delinsTC	NP_001341508.1:n.6127+83_6127+84delinsTC
XR_001740179.2:n.6408+83_6408+84delinsTC
XR_001740180.2:n.6462+83_6462+84delinsTC
XR_001740181.2:n.6341+83_6341+84delinsTC
XR_001740182.1:n.6293+83_6293+84delinsTC
XR_002959543.1:n.6518+83_6518+84delinsTC
XR_924148.2:n.6414+83_6414+84delinsTC
NM_001184.4:c.6319+83_6319+84delinsTC MANE Select	NP_001175.2:n.6319+83_6319+84delinsTC
NM_001354579.2:c.6127+83_6127+84delinsTC	NP_001341508.1:n.6127+83_6127+84delinsTC