Canonical Allele Identifier: CA1406991874

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470119C= , CM000665.2:g.142470119C=	GRCh38
NC_000003.11:g.142188961C= , CM000665.1:g.142188961C=	GRCh37
NC_000003.10:g.143671651C=	NCBI36
NG_008951.1:g.113708G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6286G= MANE Select	ENSP00000343741.4:p.Asp2096=
ENST00000513291.2:n.1470G=
ENST00000654170.1:n.1129G=
ENST00000656590.1:c.5076G=
ENST00000661310.1:c.6094G=	ENSP00000499589.1:p.Asp2032=
ENST00000665483.1:n.141G=
ENST00000666447.1:n.121G=
ENST00000666943.1:n.1750G=
ENST00000350721.8:c.6286G=	ENSP00000343741.4:p.Asp2096=
NM_001184.3:c.6286G=	NP_001175.2:p.Asp2096=
XM_011512924.1:c.6292G=	XP_011511226.1:p.Asp2098=
XM_011512925.1:c.6100G=	XP_011511227.1:p.Asp2034=
XR_924147.1:n.6381G=
XR_924148.1:n.6381G=
XR_924149.1:n.6260G=
NM_001354579.1:c.6094G=	NP_001341508.1:p.Asp2032=
XR_001740179.2:n.6375G=
XR_001740180.2:n.6429G=
XR_001740181.2:n.6308G=
XR_001740182.1:n.6260G=
XR_002959543.1:n.6485G=
XR_924148.2:n.6381G=
NM_001184.4:c.6286G= MANE Select	NP_001175.2:p.Asp2096=
NM_001354579.2:c.6094G=	NP_001341508.1:p.Asp2032=