Canonical Allele Identifier: CA1407029053

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553308G= , CM000665.2:g.142553308G=	GRCh38
NC_000003.11:g.142272150G= , CM000665.1:g.142272150G=	GRCh37
NC_000003.10:g.143754840G=	NCBI36
NG_008951.1:g.30519C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2724C= MANE Select	ENSP00000343741.4:p.Tyr908=
ENST00000515149.3:c.*1498C=	ENSP00000425897.3:n.*1498C=
ENST00000653868.1:n.2753C=
ENST00000656590.1:c.1514C=
ENST00000659195.1:n.5599C=
ENST00000661310.1:c.2532C=	ENSP00000499589.1:p.Tyr844=
ENST00000350721.8:c.2724C=	ENSP00000343741.4:p.Tyr908=
NM_001184.3:c.2724C=	NP_001175.2:p.Tyr908=
XM_011512924.1:c.2724C=	XP_011511226.1:p.Tyr908=
XM_011512925.1:c.2532C=	XP_011511227.1:p.Tyr844=
XM_011512926.1:c.2724C=	XP_011511228.1:p.Tyr908=
XM_011512927.1:c.2724C=	XP_011511229.1:p.Tyr908=
XR_924147.1:n.2813C=
XR_924148.1:n.2813C=
XR_924149.1:n.2813C=
NM_001354579.1:c.2532C=	NP_001341508.1:p.Tyr844=
XR_001740179.2:n.2813C=
XR_001740180.2:n.2813C=
XR_001740181.2:n.2813C=
XR_001740182.1:n.2813C=
XR_002959543.1:n.2813C=
XR_924148.2:n.2813C=
NM_001184.4:c.2724C= MANE Select	NP_001175.2:p.Tyr908=
NM_001354579.2:c.2532C=	NP_001341508.1:p.Tyr844=