Canonical Allele Identifier: CA1406991887

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470179G= , CM000665.2:g.142470179G=	GRCh38
NC_000003.11:g.142189021G= , CM000665.1:g.142189021G=	GRCh37
NC_000003.10:g.143671711G=	NCBI36
NG_008951.1:g.113648C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6226C= MANE Select	ENSP00000343741.4:p.Leu2076=
ENST00000513291.2:n.1410C=
ENST00000654170.1:n.1069C=
ENST00000656590.1:c.5016C=
ENST00000661310.1:c.6034C=	ENSP00000499589.1:p.Leu2012=
ENST00000665483.1:n.81C=
ENST00000666447.1:n.61C=
ENST00000666943.1:n.1690C=
ENST00000350721.8:c.6226C=	ENSP00000343741.4:p.Leu2076=
NM_001184.3:c.6226C=	NP_001175.2:p.Leu2076=
XM_011512924.1:c.6232C=	XP_011511226.1:p.Leu2078=
XM_011512925.1:c.6040C=	XP_011511227.1:p.Leu2014=
XR_924147.1:n.6321C=
XR_924148.1:n.6321C=
XR_924149.1:n.6200C=
NM_001354579.1:c.6034C=	NP_001341508.1:p.Leu2012=
XR_001740179.2:n.6315C=
XR_001740180.2:n.6369C=
XR_001740181.2:n.6248C=
XR_001740182.1:n.6200C=
XR_002959543.1:n.6425C=
XR_924148.2:n.6321C=
NM_001184.4:c.6226C= MANE Select	NP_001175.2:p.Leu2076=
NM_001354579.2:c.6034C=	NP_001341508.1:p.Leu2012=