Canonical Allele Identifier: CA1406991815

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469926_142469927delinsCT , CM000665.2:g.142469926_142469927delinsCT	GRCh38
NC_000003.11:g.142188768_142188769delinsCT , CM000665.1:g.142188768_142188769delinsCT	GRCh37
NC_000003.10:g.143671458_143671459delinsCT	NCBI36
NG_008951.1:g.113900_113901delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6319+159_6319+160delinsAG MANE Select	ENSP00000343741.4:n.6319+159_6319+160delinsAG
ENST00000513291.2:n.1503+159_1503+160delinsAG
ENST00000654170.1:n.1162+159_1162+160delinsAG
ENST00000656590.1:c.5109+159_5109+160delinsAG
ENST00000661310.1:c.6127+159_6127+160delinsAG	ENSP00000499589.1:n.6127+159_6127+160delinsAG
ENST00000665483.1:n.174+159_174+160delinsAG
ENST00000666447.1:n.154+159_154+160delinsAG
ENST00000666943.1:n.1783+159_1783+160delinsAG
ENST00000350721.8:c.6319+159_6319+160delinsAG	ENSP00000343741.4:n.6319+159_6319+160delinsAG
NM_001184.3:c.6319+159_6319+160delinsAG	NP_001175.2:n.6319+159_6319+160delinsAG
XM_011512924.1:c.6325+159_6325+160delinsAG	XP_011511226.1:n.6325+159_6325+160delinsAG
XM_011512925.1:c.6133+159_6133+160delinsAG	XP_011511227.1:n.6133+159_6133+160delinsAG
XR_924147.1:n.6414+159_6414+160delinsAG
XR_924148.1:n.6414+159_6414+160delinsAG
XR_924149.1:n.6293+159_6293+160delinsAG
NM_001354579.1:c.6127+159_6127+160delinsAG	NP_001341508.1:n.6127+159_6127+160delinsAG
XR_001740179.2:n.6408+159_6408+160delinsAG
XR_001740180.2:n.6462+159_6462+160delinsAG
XR_001740181.2:n.6341+159_6341+160delinsAG
XR_001740182.1:n.6293+159_6293+160delinsAG
XR_002959543.1:n.6518+159_6518+160delinsAG
XR_924148.2:n.6414+159_6414+160delinsAG
NM_001184.4:c.6319+159_6319+160delinsAG MANE Select	NP_001175.2:n.6319+159_6319+160delinsAG
NM_001354579.2:c.6127+159_6127+160delinsAG	NP_001341508.1:n.6127+159_6127+160delinsAG