Canonical Allele Identifier: CA1406991871

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470111A= , CM000665.2:g.142470111A=	GRCh38
NC_000003.11:g.142188953A= , CM000665.1:g.142188953A=	GRCh37
NC_000003.10:g.143671643A=	NCBI36
NG_008951.1:g.113716T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6294T= MANE Select	ENSP00000343741.4:p.Gly2098=
ENST00000513291.2:n.1478T=
ENST00000654170.1:n.1137T=
ENST00000656590.1:c.5084T=
ENST00000661310.1:c.6102T=	ENSP00000499589.1:p.Gly2034=
ENST00000665483.1:n.149T=
ENST00000666447.1:n.129T=
ENST00000666943.1:n.1758T=
ENST00000350721.8:c.6294T=	ENSP00000343741.4:p.Gly2098=
NM_001184.3:c.6294T=	NP_001175.2:p.Gly2098=
XM_011512924.1:c.6300T=	XP_011511226.1:p.Gly2100=
XM_011512925.1:c.6108T=	XP_011511227.1:p.Gly2036=
XR_924147.1:n.6389T=
XR_924148.1:n.6389T=
XR_924149.1:n.6268T=
NM_001354579.1:c.6102T=	NP_001341508.1:p.Gly2034=
XR_001740179.2:n.6383T=
XR_001740180.2:n.6437T=
XR_001740181.2:n.6316T=
XR_001740182.1:n.6268T=
XR_002959543.1:n.6493T=
XR_924148.2:n.6389T=
NM_001184.4:c.6294T= MANE Select	NP_001175.2:p.Gly2098=
NM_001354579.2:c.6102T=	NP_001341508.1:p.Gly2034=