Canonical Allele Identifier: CA1407006926

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142498619G= , CM000665.2:g.142498619G=	GRCh38
NC_000003.11:g.142217461G= , CM000665.1:g.142217461G=	GRCh37
NC_000003.10:g.143700151G=	NCBI36
NG_008951.1:g.85208C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.5536C= MANE Select	ENSP00000343741.4:p.Arg1846=
ENST00000513291.2:n.720C=
ENST00000653868.1:n.5565C=
ENST00000656590.1:c.4326C=
ENST00000661310.1:c.5344C=	ENSP00000499589.1:p.Arg1782=
ENST00000666943.1:n.1000C=
ENST00000350721.8:c.5536C=	ENSP00000343741.4:p.Arg1846=
ENST00000507620.2:n.632C=
ENST00000514393.5:n.219C=
NM_001184.3:c.5536C=	NP_001175.2:p.Arg1846=
XM_011512924.1:c.5542C=	XP_011511226.1:p.Arg1848=
XM_011512925.1:c.5350C=	XP_011511227.1:p.Arg1784=
XM_011512926.1:c.5542C=	XP_011511228.1:p.Arg1848=
XM_011512927.1:c.5542C=	XP_011511229.1:p.Arg1848=
XR_924147.1:n.5631C=
XR_924148.1:n.5631C=
XR_924149.1:n.5631C=
NM_001354579.1:c.5344C=	NP_001341508.1:p.Arg1782=
XR_001740179.2:n.5625C=
XR_001740180.2:n.5631C=
XR_001740181.2:n.5631C=
XR_001740182.1:n.5631C=
XR_002959543.1:n.5631C=
XR_924148.2:n.5631C=
NM_001184.4:c.5536C= MANE Select	NP_001175.2:p.Arg1846=
NM_001354579.2:c.5344C=	NP_001341508.1:p.Arg1782=