Canonical Allele Identifier: CA2650253

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142550231C>T , CM000665.2:g.142550231C>T	GRCh38
NC_000003.11:g.142269073C>T , CM000665.1:g.142269073C>T	GRCh37
NC_000003.10:g.143751763C>T	NCBI36
NG_008951.1:g.33596G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.2877G>A MANE Select	NP_001175.2:p.Val959=
ENST00000350721.9:c.2877G>A MANE Select	ENSP00000343741.4:p.Val959=
NM_001184.3:c.2877G>A	NP_001175.2:p.Val959=
NM_001354579.1:c.2685G>A	NP_001341508.1:p.Val895=
NM_001354579.2:c.2685G>A	NP_001341508.1:p.Val895=
ENST00000350721.8:c.2877G>A	ENSP00000343741.4:p.Val959=
ENST00000515149.3:c.*1651G>A	ENSP00000425897.3:n.*1651G>A
ENST00000653868.1:n.2906G>A
ENST00000656582.1:n.136G>A
ENST00000656590.1:c.1667G>A
ENST00000659195.1:n.5752G>A
ENST00000661310.1:c.2685G>A	ENSP00000499589.1:p.Val895=
XM_011512924.1:c.2877G>A	XP_011511226.1:p.Val959=
XM_011512925.1:c.2685G>A	XP_011511227.1:p.Val895=
XM_011512926.1:c.2877G>A	XP_011511228.1:p.Val959=
XM_011512927.1:c.2877G>A	XP_011511229.1:p.Val959=
XR_001740179.2:n.2966G>A
XR_001740180.2:n.2966G>A
XR_001740181.2:n.2966G>A
XR_001740182.1:n.2966G>A
XR_002959543.1:n.2966G>A
XR_924147.1:n.2966G>A
XR_924148.1:n.2966G>A
XR_924148.2:n.2966G>A
XR_924149.1:n.2966G>A