Canonical Allele Identifier: CA1407011025

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513467A= , CM000665.2:g.142513467A=	GRCh38
NC_000003.11:g.142232309A= , CM000665.1:g.142232309A=	GRCh37
NC_000003.10:g.143714999A=	NCBI36
NG_008951.1:g.70360T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4641+34T= MANE Select	ENSP00000343741.4:n.4641+34T=
ENST00000653868.1:n.4670+34T=
ENST00000656590.1:c.3431+34T=
ENST00000661310.1:c.4449+34T=	ENSP00000499589.1:n.4449+34T=
ENST00000666943.1:n.105+34T=
ENST00000350721.8:c.4641+34T=	ENSP00000343741.4:n.4641+34T=
NM_001184.3:c.4641+34T=	NP_001175.2:n.4641+34T=
XM_011512924.1:c.4647+34T=	XP_011511226.1:n.4647+34T=
XM_011512925.1:c.4455+34T=	XP_011511227.1:n.4455+34T=
XM_011512926.1:c.4647+34T=	XP_011511228.1:n.4647+34T=
XM_011512927.1:c.4647+34T=	XP_011511229.1:n.4647+34T=
XR_924147.1:n.4736+34T=
XR_924148.1:n.4736+34T=
XR_924149.1:n.4736+34T=
NM_001354579.1:c.4449+34T=	NP_001341508.1:n.4449+34T=
XR_001740179.2:n.4730+34T=
XR_001740180.2:n.4736+34T=
XR_001740181.2:n.4736+34T=
XR_001740182.1:n.4736+34T=
XR_002959543.1:n.4736+34T=
XR_924148.2:n.4736+34T=
NM_001184.4:c.4641+34T= MANE Select	NP_001175.2:n.4641+34T=
NM_001354579.2:c.4449+34T=	NP_001341508.1:n.4449+34T=