Canonical Allele Identifier: CA1406978009

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449591A= , CM000665.2:g.142449591A=	GRCh38
NC_000003.11:g.142168433A= , CM000665.1:g.142168433A=	GRCh37
NC_000003.10:g.143651123A=	NCBI36
NG_008951.1:g.134236T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7773T= MANE Select	ENSP00000343741.4:p.His2591=
ENST00000513291.2:n.6482T=
ENST00000653893.1:n.2631T=
ENST00000654170.1:n.2616T=
ENST00000656114.1:n.2859T=
ENST00000656590.1:c.6700T=
ENST00000658083.1:n.2953T=
ENST00000661310.1:c.7581T=	ENSP00000499589.1:p.His2527=
ENST00000665483.1:n.5313T=
ENST00000666447.1:n.4276T=
ENST00000666943.1:n.4505T=
ENST00000350721.8:c.7773T=	ENSP00000343741.4:p.His2591=
ENST00000504521.5:c.362T=	ENSP00000422553.1:n.362T=
ENST00000513291.1:c.4837T=
ENST00000515810.1:c.199T=	ENSP00000421870.1:n.199T=
NM_001184.3:c.7773T=	NP_001175.2:p.His2591=
XM_011512924.1:c.7779T=	XP_011511226.1:p.His2593=
XM_011512925.1:c.7587T=	XP_011511227.1:p.His2529=
XR_924147.1:n.10530T=
XR_924148.1:n.8005T=
NM_001354579.1:c.7581T=	NP_001341508.1:p.His2527=
XR_001740179.2:n.7999T=
XR_924148.2:n.8005T=
NM_001184.4:c.7773T= MANE Select	NP_001175.2:p.His2591=
NM_001354579.2:c.7581T=	NP_001341508.1:p.His2527=