Canonical Allele Identifier: CA436106428

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142232385C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513543C>T , CM000665.2:g.142513543C>T	GRCh38
NC_000003.11:g.142232385C>T , CM000665.1:g.142232385C>T	GRCh37
NC_000003.10:g.143715075C>T	NCBI36
NG_008951.1:g.70284G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4599G>A MANE Select	ENSP00000343741.4:p.Leu1533=
ENST00000653868.1:n.4628G>A
ENST00000656590.1:c.3389G>A
ENST00000661310.1:c.4407G>A	ENSP00000499589.1:p.Leu1469=
ENST00000666943.1:n.63G>A
ENST00000350721.8:c.4599G>A	ENSP00000343741.4:p.Leu1533=
NM_001184.3:c.4599G>A	NP_001175.2:p.Leu1533=
XM_011512924.1:c.4605G>A	XP_011511226.1:p.Leu1535=
XM_011512925.1:c.4413G>A	XP_011511227.1:p.Leu1471=
XM_011512926.1:c.4605G>A	XP_011511228.1:p.Leu1535=
XM_011512927.1:c.4605G>A	XP_011511229.1:p.Leu1535=
XR_924147.1:n.4694G>A
XR_924148.1:n.4694G>A
XR_924149.1:n.4694G>A
NM_001354579.1:c.4407G>A	NP_001341508.1:p.Leu1469=
XR_001740179.2:n.4688G>A
XR_001740180.2:n.4694G>A
XR_001740181.2:n.4694G>A
XR_001740182.1:n.4694G>A
XR_002959543.1:n.4694G>A
XR_924148.2:n.4694G>A
NM_001184.4:c.4599G>A MANE Select	NP_001175.2:p.Leu1533=
NM_001354579.2:c.4407G>A	NP_001341508.1:p.Leu1469=