Canonical Allele Identifier: CA1406991879

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470139C= , CM000665.2:g.142470139C=	GRCh38
NC_000003.11:g.142188981C= , CM000665.1:g.142188981C=	GRCh37
NC_000003.10:g.143671671C=	NCBI36
NG_008951.1:g.113688G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6266G= MANE Select	ENSP00000343741.4:p.Arg2089=
ENST00000513291.2:n.1450G=
ENST00000654170.1:n.1109G=
ENST00000656590.1:c.5056G=
ENST00000661310.1:c.6074G=	ENSP00000499589.1:p.Arg2025=
ENST00000665483.1:n.121G=
ENST00000666447.1:n.101G=
ENST00000666943.1:n.1730G=
ENST00000350721.8:c.6266G=	ENSP00000343741.4:p.Arg2089=
NM_001184.3:c.6266G=	NP_001175.2:p.Arg2089=
XM_011512924.1:c.6272G=	XP_011511226.1:p.Arg2091=
XM_011512925.1:c.6080G=	XP_011511227.1:p.Arg2027=
XR_924147.1:n.6361G=
XR_924148.1:n.6361G=
XR_924149.1:n.6240G=
NM_001354579.1:c.6074G=	NP_001341508.1:p.Arg2025=
XR_001740179.2:n.6355G=
XR_001740180.2:n.6409G=
XR_001740181.2:n.6288G=
XR_001740182.1:n.6240G=
XR_002959543.1:n.6465G=
XR_924148.2:n.6361G=
NM_001184.4:c.6266G= MANE Select	NP_001175.2:p.Arg2089=
NM_001354579.2:c.6074G=	NP_001341508.1:p.Arg2025=