Canonical Allele Identifier: CA436125972

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188971A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470129A>T , CM000665.2:g.142470129A>T	GRCh38
NC_000003.11:g.142188971A>T , CM000665.1:g.142188971A>T	GRCh37
NC_000003.10:g.143671661A>T	NCBI36
NG_008951.1:g.113698T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6276T>A MANE Select	ENSP00000343741.4:p.Thr2092=
ENST00000513291.2:n.1460T>A
ENST00000654170.1:n.1119T>A
ENST00000656590.1:c.5066T>A
ENST00000661310.1:c.6084T>A	ENSP00000499589.1:p.Thr2028=
ENST00000665483.1:n.131T>A
ENST00000666447.1:n.111T>A
ENST00000666943.1:n.1740T>A
ENST00000350721.8:c.6276T>A	ENSP00000343741.4:p.Thr2092=
NM_001184.3:c.6276T>A	NP_001175.2:p.Thr2092=
XM_011512924.1:c.6282T>A	XP_011511226.1:p.Thr2094=
XM_011512925.1:c.6090T>A	XP_011511227.1:p.Thr2030=
XR_924147.1:n.6371T>A
XR_924148.1:n.6371T>A
XR_924149.1:n.6250T>A
NM_001354579.1:c.6084T>A	NP_001341508.1:p.Thr2028=
XR_001740179.2:n.6365T>A
XR_001740180.2:n.6419T>A
XR_001740181.2:n.6298T>A
XR_001740182.1:n.6250T>A
XR_002959543.1:n.6475T>A
XR_924148.2:n.6371T>A
NM_001184.4:c.6276T>A MANE Select	NP_001175.2:p.Thr2092=
NM_001354579.2:c.6084T>A	NP_001341508.1:p.Thr2028=