Canonical Allele Identifier: CA1407011081

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513613A= , CM000665.2:g.142513613A=	GRCh38
NC_000003.11:g.142232455A= , CM000665.1:g.142232455A=	GRCh37
NC_000003.10:g.143715145A=	NCBI36
NG_008951.1:g.70214T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4529T= MANE Select	ENSP00000343741.4:p.Ile1510=
ENST00000653868.1:n.4558T=
ENST00000656590.1:c.3319T=
ENST00000661310.1:c.4337T=	ENSP00000499589.1:p.Ile1446=
ENST00000350721.8:c.4529T=	ENSP00000343741.4:p.Ile1510=
NM_001184.3:c.4529T=	NP_001175.2:p.Ile1510=
XM_011512924.1:c.4535T=	XP_011511226.1:p.Ile1512=
XM_011512925.1:c.4343T=	XP_011511227.1:p.Ile1448=
XM_011512926.1:c.4535T=	XP_011511228.1:p.Ile1512=
XM_011512927.1:c.4535T=	XP_011511229.1:p.Ile1512=
XR_924147.1:n.4624T=
XR_924148.1:n.4624T=
XR_924149.1:n.4624T=
NM_001354579.1:c.4337T=	NP_001341508.1:p.Ile1446=
XR_001740179.2:n.4618T=
XR_001740180.2:n.4624T=
XR_001740181.2:n.4624T=
XR_001740182.1:n.4624T=
XR_002959543.1:n.4624T=
XR_924148.2:n.4624T=
NM_001184.4:c.4529T= MANE Select	NP_001175.2:p.Ile1510=
NM_001354579.2:c.4337T=	NP_001341508.1:p.Ile1446=