Canonical Allele Identifier: CA1406978001

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449572G= , CM000665.2:g.142449572G=	GRCh38
NC_000003.11:g.142168414G= , CM000665.1:g.142168414G=	GRCh37
NC_000003.10:g.143651104G=	NCBI36
NG_008951.1:g.134255C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7792C= MANE Select	ENSP00000343741.4:p.Arg2598=
ENST00000513291.2:n.6501C=
ENST00000653893.1:n.2650C=
ENST00000654170.1:n.2635C=
ENST00000656114.1:n.2878C=
ENST00000656590.1:c.6719C=
ENST00000658083.1:n.2972C=
ENST00000661310.1:c.7600C=	ENSP00000499589.1:p.Arg2534=
ENST00000665483.1:n.5332C=
ENST00000666447.1:n.4295C=
ENST00000666943.1:n.4524C=
ENST00000350721.8:c.7792C=	ENSP00000343741.4:p.Arg2598=
ENST00000504521.5:c.381C=	ENSP00000422553.1:n.381C=
ENST00000513291.1:c.4856C=
ENST00000515810.1:c.218C=	ENSP00000421870.1:n.218C=
NM_001184.3:c.7792C=	NP_001175.2:p.Arg2598=
XM_011512924.1:c.7798C=	XP_011511226.1:p.Arg2600=
XM_011512925.1:c.7606C=	XP_011511227.1:p.Arg2536=
XR_924147.1:n.10549C=
XR_924148.1:n.8024C=
NM_001354579.1:c.7600C=	NP_001341508.1:p.Arg2534=
XR_001740179.2:n.8018C=
XR_924148.2:n.8024C=
NM_001184.4:c.7792C= MANE Select	NP_001175.2:p.Arg2598=
NM_001354579.2:c.7600C=	NP_001341508.1:p.Arg2534=