Canonical Allele Identifier: CA1406991771

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469835_142469836delinsCA , CM000665.2:g.142469835_142469836delinsCA	GRCh38
NC_000003.11:g.142188677_142188678delinsCA , CM000665.1:g.142188677_142188678delinsCA	GRCh37
NC_000003.10:g.143671367_143671368delinsCA	NCBI36
NG_008951.1:g.113991_113992delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6319+250_6319+251delinsTG MANE Select	ENSP00000343741.4:n.6319+250_6319+251delinsTG
ENST00000513291.2:n.1503+250_1503+251delinsTG
ENST00000654170.1:n.1162+250_1162+251delinsTG
ENST00000656590.1:c.5109+250_5109+251delinsTG
ENST00000661310.1:c.6127+250_6127+251delinsTG	ENSP00000499589.1:n.6127+250_6127+251delinsTG
ENST00000665483.1:n.174+250_174+251delinsTG
ENST00000666447.1:n.154+250_154+251delinsTG
ENST00000666943.1:n.1783+250_1783+251delinsTG
ENST00000350721.8:c.6319+250_6319+251delinsTG	ENSP00000343741.4:n.6319+250_6319+251delinsTG
NM_001184.3:c.6319+250_6319+251delinsTG	NP_001175.2:n.6319+250_6319+251delinsTG
XM_011512924.1:c.6325+250_6325+251delinsTG	XP_011511226.1:n.6325+250_6325+251delinsTG
XM_011512925.1:c.6133+250_6133+251delinsTG	XP_011511227.1:n.6133+250_6133+251delinsTG
XR_924147.1:n.6414+250_6414+251delinsTG
XR_924148.1:n.6414+250_6414+251delinsTG
XR_924149.1:n.6293+250_6293+251delinsTG
NM_001354579.1:c.6127+250_6127+251delinsTG	NP_001341508.1:n.6127+250_6127+251delinsTG
XR_001740179.2:n.6408+250_6408+251delinsTG
XR_001740180.2:n.6462+250_6462+251delinsTG
XR_001740181.2:n.6341+250_6341+251delinsTG
XR_001740182.1:n.6293+250_6293+251delinsTG
XR_002959543.1:n.6518+250_6518+251delinsTG
XR_924148.2:n.6414+250_6414+251delinsTG
NM_001184.4:c.6319+250_6319+251delinsTG MANE Select	NP_001175.2:n.6319+250_6319+251delinsTG
NM_001354579.2:c.6127+250_6127+251delinsTG	NP_001341508.1:n.6127+250_6127+251delinsTG