Canonical Allele Identifier: CA1407011051

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513526C= , CM000665.2:g.142513526C=	GRCh38
NC_000003.11:g.142232368C= , CM000665.1:g.142232368C=	GRCh37
NC_000003.10:g.143715058C=	NCBI36
NG_008951.1:g.70301G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4616G= MANE Select	ENSP00000343741.4:p.Gly1539=
ENST00000653868.1:n.4645G=
ENST00000656590.1:c.3406G=
ENST00000661310.1:c.4424G=	ENSP00000499589.1:p.Gly1475=
ENST00000666943.1:n.80G=
ENST00000350721.8:c.4616G=	ENSP00000343741.4:p.Gly1539=
NM_001184.3:c.4616G=	NP_001175.2:p.Gly1539=
XM_011512924.1:c.4622G=	XP_011511226.1:p.Gly1541=
XM_011512925.1:c.4430G=	XP_011511227.1:p.Gly1477=
XM_011512926.1:c.4622G=	XP_011511228.1:p.Gly1541=
XM_011512927.1:c.4622G=	XP_011511229.1:p.Gly1541=
XR_924147.1:n.4711G=
XR_924148.1:n.4711G=
XR_924149.1:n.4711G=
NM_001354579.1:c.4424G=	NP_001341508.1:p.Gly1475=
XR_001740179.2:n.4705G=
XR_001740180.2:n.4711G=
XR_001740181.2:n.4711G=
XR_001740182.1:n.4711G=
XR_002959543.1:n.4711G=
XR_924148.2:n.4711G=
NM_001184.4:c.4616G= MANE Select	NP_001175.2:p.Gly1539=
NM_001354579.2:c.4424G=	NP_001341508.1:p.Gly1475=