Canonical Allele Identifier: CA1406991615

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469458T= , CM000665.2:g.142469458T=	GRCh38
NC_000003.11:g.142188300T= , CM000665.1:g.142188300T=	GRCh37
NC_000003.10:g.143670990T=	NCBI36
NG_008951.1:g.114369A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6431A= MANE Select	ENSP00000343741.4:p.Gln2144=
ENST00000513291.2:n.1615A=
ENST00000654170.1:n.1274A=
ENST00000656590.1:c.5221A=
ENST00000661310.1:c.6239A=	ENSP00000499589.1:p.Gln2080=
ENST00000665483.1:n.286A=
ENST00000666447.1:n.266A=
ENST00000666943.1:n.1895A=
ENST00000350721.8:c.6431A=	ENSP00000343741.4:p.Gln2144=
NM_001184.3:c.6431A=	NP_001175.2:p.Gln2144=
XM_011512924.1:c.6437A=	XP_011511226.1:p.Gln2146=
XM_011512925.1:c.6245A=	XP_011511227.1:p.Gln2082=
XR_924147.1:n.6526A=
XR_924148.1:n.6526A=
XR_924149.1:n.6405A=
NM_001354579.1:c.6239A=	NP_001341508.1:p.Gln2080=
XR_001740179.2:n.6520A=
XR_924148.2:n.6526A=
NM_001184.4:c.6431A= MANE Select	NP_001175.2:p.Gln2144=
NM_001354579.2:c.6239A=	NP_001341508.1:p.Gln2080=