Canonical Allele Identifier: CA1406978027

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449601G= , CM000665.2:g.142449601G=	GRCh38
NC_000003.11:g.142168443G= , CM000665.1:g.142168443G=	GRCh37
NC_000003.10:g.143651133G=	NCBI36
NG_008951.1:g.134226C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7763C= MANE Select	ENSP00000343741.4:p.Ala2588=
ENST00000513291.2:n.6472C=
ENST00000653893.1:n.2621C=
ENST00000654170.1:n.2606C=
ENST00000656114.1:n.2849C=
ENST00000656590.1:c.6690C=
ENST00000658083.1:n.2943C=
ENST00000661310.1:c.7571C=	ENSP00000499589.1:p.Ala2524=
ENST00000665483.1:n.5303C=
ENST00000666447.1:n.4266C=
ENST00000666943.1:n.4495C=
ENST00000350721.8:c.7763C=	ENSP00000343741.4:p.Ala2588=
ENST00000504521.5:c.352C=	ENSP00000422553.1:n.352C=
ENST00000513291.1:c.4827C=
ENST00000515810.1:c.189C=	ENSP00000421870.1:n.189C=
NM_001184.3:c.7763C=	NP_001175.2:p.Ala2588=
XM_011512924.1:c.7769C=	XP_011511226.1:p.Ala2590=
XM_011512925.1:c.7577C=	XP_011511227.1:p.Ala2526=
XR_924147.1:n.10520C=
XR_924148.1:n.7995C=
NM_001354579.1:c.7571C=	NP_001341508.1:p.Ala2524=
XR_001740179.2:n.7989C=
XR_924148.2:n.7995C=
NM_001184.4:c.7763C= MANE Select	NP_001175.2:p.Ala2588=
NM_001354579.2:c.7571C=	NP_001341508.1:p.Ala2524=