Canonical Allele Identifier: CA1407006352

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142497116C= , CM000665.2:g.142497116C=	GRCh38
NC_000003.11:g.142215958C= , CM000665.1:g.142215958C=	GRCh37
NC_000003.10:g.143698648C=	NCBI36
NG_008951.1:g.86711G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.5635G= MANE Select	ENSP00000343741.4:p.Asp1879=
ENST00000513291.2:n.819G=
ENST00000653868.1:n.5664G=
ENST00000656590.1:c.4425G=
ENST00000661310.1:c.5443G=	ENSP00000499589.1:p.Asp1815=
ENST00000666943.1:n.1099G=
ENST00000350721.8:c.5635G=	ENSP00000343741.4:p.Asp1879=
ENST00000507620.2:n.713+18G=
ENST00000514393.5:n.318G=
NM_001184.3:c.5635G=	NP_001175.2:p.Asp1879=
XM_011512924.1:c.5641G=	XP_011511226.1:p.Asp1881=
XM_011512925.1:c.5449G=	XP_011511227.1:p.Asp1817=
XM_011512926.1:c.5641G=	XP_011511228.1:p.Asp1881=
XM_011512927.1:c.5641G=	XP_011511229.1:p.Asp1881=
XR_924147.1:n.5730G=
XR_924148.1:n.5730G=
XR_924149.1:n.5712+18G=
NM_001354579.1:c.5443G=	NP_001341508.1:p.Asp1815=
XR_001740179.2:n.5724G=
XR_001740180.2:n.5730G=
XR_001740181.2:n.5712+18G=
XR_001740182.1:n.5712+18G=
XR_002959543.1:n.5730G=
XR_924148.2:n.5730G=
NM_001184.4:c.5635G= MANE Select	NP_001175.2:p.Asp1879=
NM_001354579.2:c.5443G=	NP_001341508.1:p.Asp1815=