Canonical Allele Identifier: CA1407014947

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142522760G= , CM000665.2:g.142522760G=	GRCh38
NC_000003.11:g.142241602G= , CM000665.1:g.142241602G=	GRCh37
NC_000003.10:g.143724292G=	NCBI36
NG_008951.1:g.61067C=

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.4234C= MANE Select	NP_001175.2:p.Arg1412=
ENST00000350721.9:c.4234C= MANE Select	ENSP00000343741.4:p.Arg1412=
NM_001184.3:c.4234C=	NP_001175.2:p.Arg1412=
NM_001354579.1:c.4042C=	NP_001341508.1:p.Arg1348=
NM_001354579.2:c.4042C=	NP_001341508.1:p.Arg1348=
ENST00000350721.8:c.4234C=	ENSP00000343741.4:p.Arg1412=
ENST00000653868.1:n.4263C=
ENST00000656590.1:c.3024C=
ENST00000661310.1:c.4042C=	ENSP00000499589.1:p.Arg1348=
XM_011512924.1:c.4240C=	XP_011511226.1:p.Arg1414=
XM_011512925.1:c.4048C=	XP_011511227.1:p.Arg1350=
XM_011512926.1:c.4240C=	XP_011511228.1:p.Arg1414=
XM_011512927.1:c.4240C=	XP_011511229.1:p.Arg1414=
XR_001740179.2:n.4323C=
XR_001740180.2:n.4329C=
XR_001740181.2:n.4329C=
XR_001740182.1:n.4329C=
XR_002959543.1:n.4329C=
XR_924147.1:n.4329C=
XR_924148.1:n.4329C=
XR_924148.2:n.4329C=
XR_924149.1:n.4329C=