Canonical Allele Identifier: CA1406977969

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449548G= , CM000665.2:g.142449548G=	GRCh38
NC_000003.11:g.142168390G= , CM000665.1:g.142168390G=	GRCh37
NC_000003.10:g.143651080G=	NCBI36
NG_008951.1:g.134279C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7816C= MANE Select	ENSP00000343741.4:p.Arg2606=
ENST00000513291.2:n.6525C=
ENST00000653893.1:n.2674C=
ENST00000654170.1:n.2659C=
ENST00000656114.1:n.2902C=
ENST00000656590.1:c.6743C=
ENST00000658083.1:n.2996C=
ENST00000661310.1:c.7624C=	ENSP00000499589.1:p.Arg2542=
ENST00000665483.1:n.5356C=
ENST00000666447.1:n.4319C=
ENST00000666943.1:n.4548C=
ENST00000350721.8:c.7816C=	ENSP00000343741.4:p.Arg2606=
ENST00000504521.5:c.405C=	ENSP00000422553.1:n.405C=
ENST00000513291.1:c.4880C=
ENST00000515810.1:c.242C=	ENSP00000421870.1:n.242C=
NM_001184.3:c.7816C=	NP_001175.2:p.Arg2606=
XM_011512924.1:c.7822C=	XP_011511226.1:p.Arg2608=
XM_011512925.1:c.7630C=	XP_011511227.1:p.Arg2544=
XR_924147.1:n.10573C=
XR_924148.1:n.8048C=
NM_001354579.1:c.7624C=	NP_001341508.1:p.Arg2542=
XR_001740179.2:n.8042C=
XR_924148.2:n.8048C=
NM_001184.4:c.7816C= MANE Select	NP_001175.2:p.Arg2606=
NM_001354579.2:c.7624C=	NP_001341508.1:p.Arg2542=