Canonical Allele Identifier: CA1407011082

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513617T= , CM000665.2:g.142513617T=	GRCh38
NC_000003.11:g.142232459T= , CM000665.1:g.142232459T=	GRCh37
NC_000003.10:g.143715149T=	NCBI36
NG_008951.1:g.70210A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4525A= MANE Select	ENSP00000343741.4:p.Lys1509=
ENST00000653868.1:n.4554A=
ENST00000656590.1:c.3315A=
ENST00000661310.1:c.4333A=	ENSP00000499589.1:p.Lys1445=
ENST00000350721.8:c.4525A=	ENSP00000343741.4:p.Lys1509=
NM_001184.3:c.4525A=	NP_001175.2:p.Lys1509=
XM_011512924.1:c.4531A=	XP_011511226.1:p.Lys1511=
XM_011512925.1:c.4339A=	XP_011511227.1:p.Lys1447=
XM_011512926.1:c.4531A=	XP_011511228.1:p.Lys1511=
XM_011512927.1:c.4531A=	XP_011511229.1:p.Lys1511=
XR_924147.1:n.4620A=
XR_924148.1:n.4620A=
XR_924149.1:n.4620A=
NM_001354579.1:c.4333A=	NP_001341508.1:p.Lys1445=
XR_001740179.2:n.4614A=
XR_001740180.2:n.4620A=
XR_001740181.2:n.4620A=
XR_001740182.1:n.4620A=
XR_002959543.1:n.4620A=
XR_924148.2:n.4620A=
NM_001184.4:c.4525A= MANE Select	NP_001175.2:p.Lys1509=
NM_001354579.2:c.4333A=	NP_001341508.1:p.Lys1445=