Canonical Allele Identifier: CA1406991588

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469367T= , CM000665.2:g.142469367T=	GRCh38
NC_000003.11:g.142188209T= , CM000665.1:g.142188209T=	GRCh37
NC_000003.10:g.143670899T=	NCBI36
NG_008951.1:g.114460A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6522A= MANE Select	ENSP00000343741.4:p.Gln2174=
ENST00000513291.2:n.1706A=
ENST00000654170.1:n.1365A=
ENST00000656590.1:c.5312A=
ENST00000661310.1:c.6330A=	ENSP00000499589.1:p.Gln2110=
ENST00000665483.1:n.377A=
ENST00000666447.1:n.357A=
ENST00000666943.1:n.1986A=
ENST00000350721.8:c.6522A=	ENSP00000343741.4:p.Gln2174=
ENST00000513291.1:c.61A=
NM_001184.3:c.6522A=	NP_001175.2:p.Gln2174=
XM_011512924.1:c.6528A=	XP_011511226.1:p.Gln2176=
XM_011512925.1:c.6336A=	XP_011511227.1:p.Gln2112=
XR_924147.1:n.6617A=
XR_924148.1:n.6617A=
XR_924149.1:n.6496A=
NM_001354579.1:c.6330A=	NP_001341508.1:p.Gln2110=
XR_001740179.2:n.6611A=
XR_924148.2:n.6617A=
NM_001184.4:c.6522A= MANE Select	NP_001175.2:p.Gln2174=
NM_001354579.2:c.6330A=	NP_001341508.1:p.Gln2110=