Canonical Allele Identifier: CA1406991595

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469396C= , CM000665.2:g.142469396C=	GRCh38
NC_000003.11:g.142188238C= , CM000665.1:g.142188238C=	GRCh37
NC_000003.10:g.143670928C=	NCBI36
NG_008951.1:g.114431G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6493G= MANE Select	ENSP00000343741.4:p.Ala2165=
ENST00000513291.2:n.1677G=
ENST00000654170.1:n.1336G=
ENST00000656590.1:c.5283G=
ENST00000661310.1:c.6301G=	ENSP00000499589.1:p.Ala2101=
ENST00000665483.1:n.348G=
ENST00000666447.1:n.328G=
ENST00000666943.1:n.1957G=
ENST00000350721.8:c.6493G=	ENSP00000343741.4:p.Ala2165=
ENST00000513291.1:c.32G=
NM_001184.3:c.6493G=	NP_001175.2:p.Ala2165=
XM_011512924.1:c.6499G=	XP_011511226.1:p.Ala2167=
XM_011512925.1:c.6307G=	XP_011511227.1:p.Ala2103=
XR_924147.1:n.6588G=
XR_924148.1:n.6588G=
XR_924149.1:n.6467G=
NM_001354579.1:c.6301G=	NP_001341508.1:p.Ala2101=
XR_001740179.2:n.6582G=
XR_924148.2:n.6588G=
NM_001184.4:c.6493G= MANE Select	NP_001175.2:p.Ala2165=
NM_001354579.2:c.6301G=	NP_001341508.1:p.Ala2101=