Canonical Allele Identifier: CA1406991877

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470131T= , CM000665.2:g.142470131T=	GRCh38
NC_000003.11:g.142188973T= , CM000665.1:g.142188973T=	GRCh37
NC_000003.10:g.143671663T=	NCBI36
NG_008951.1:g.113696A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6274A= MANE Select	ENSP00000343741.4:p.Thr2092=
ENST00000513291.2:n.1458A=
ENST00000654170.1:n.1117A=
ENST00000656590.1:c.5064A=
ENST00000661310.1:c.6082A=	ENSP00000499589.1:p.Thr2028=
ENST00000665483.1:n.129A=
ENST00000666447.1:n.109A=
ENST00000666943.1:n.1738A=
ENST00000350721.8:c.6274A=	ENSP00000343741.4:p.Thr2092=
NM_001184.3:c.6274A=	NP_001175.2:p.Thr2092=
XM_011512924.1:c.6280A=	XP_011511226.1:p.Thr2094=
XM_011512925.1:c.6088A=	XP_011511227.1:p.Thr2030=
XR_924147.1:n.6369A=
XR_924148.1:n.6369A=
XR_924149.1:n.6248A=
NM_001354579.1:c.6082A=	NP_001341508.1:p.Thr2028=
XR_001740179.2:n.6363A=
XR_001740180.2:n.6417A=
XR_001740181.2:n.6296A=
XR_001740182.1:n.6248A=
XR_002959543.1:n.6473A=
XR_924148.2:n.6369A=
NM_001184.4:c.6274A= MANE Select	NP_001175.2:p.Thr2092=
NM_001354579.2:c.6082A=	NP_001341508.1:p.Thr2028=