Canonical Allele Identifier: CA1407028963

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553231_142553233delinsCAG , CM000665.2:g.142553231_142553233delinsCAG	GRCh38
NC_000003.11:g.142272073_142272075delinsCAG , CM000665.1:g.142272073_142272075delinsCAG	GRCh37
NC_000003.10:g.143754763_143754765delinsCAG	NCBI36
NG_008951.1:g.30594_30596delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2799_2801delinsCTG MANE Select	ENSP00000343741.4:p.Ile933=
ENST00000515149.3:c.*1573_*1575delinsCTG	ENSP00000425897.3:n.*1573_*1575delinsCTG
ENST00000653868.1:n.2828_2830delinsCTG
ENST00000656582.1:n.58_60delinsCTG
ENST00000656590.1:c.1589_1591delinsCTG
ENST00000659195.1:n.5674_5676delinsCTG
ENST00000661310.1:c.2607_2609delinsCTG	ENSP00000499589.1:p.Ile869=
ENST00000350721.8:c.2799_2801delinsCTG	ENSP00000343741.4:p.Ile933=
NM_001184.3:c.2799_2801delinsCTG	NP_001175.2:p.Ile933=
XM_011512924.1:c.2799_2801delinsCTG	XP_011511226.1:p.Ile933=
XM_011512925.1:c.2607_2609delinsCTG	XP_011511227.1:p.Ile869=
XM_011512926.1:c.2799_2801delinsCTG	XP_011511228.1:p.Ile933=
XM_011512927.1:c.2799_2801delinsCTG	XP_011511229.1:p.Ile933=
XR_924147.1:n.2888_2890delinsCTG
XR_924148.1:n.2888_2890delinsCTG
XR_924149.1:n.2888_2890delinsCTG
NM_001354579.1:c.2607_2609delinsCTG	NP_001341508.1:p.Ile869=
XR_001740179.2:n.2888_2890delinsCTG
XR_001740180.2:n.2888_2890delinsCTG
XR_001740181.2:n.2888_2890delinsCTG
XR_001740182.1:n.2888_2890delinsCTG
XR_002959543.1:n.2888_2890delinsCTG
XR_924148.2:n.2888_2890delinsCTG
NM_001184.4:c.2799_2801delinsCTG MANE Select	NP_001175.2:p.Ile933=
NM_001354579.2:c.2607_2609delinsCTG	NP_001341508.1:p.Ile869=