Canonical Allele Identifier: CA84733812

Gene: ATR

Linked Data

• dbSNP Id: rs1032148842
• COSMIC: COSM5008772
• MyVariant Identifiers: chr3:g.142188981C>T (hg19) ; chr3:g.142470139C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470139C>T , CM000665.2:g.142470139C>T	GRCh38
NC_000003.11:g.142188981C>T , CM000665.1:g.142188981C>T	GRCh37
NC_000003.10:g.143671671C>T	NCBI36
NG_008951.1:g.113688G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6266G>A MANE Select	ENSP00000343741.4:p.Arg2089Gln
ENST00000513291.2:n.1450G>A
ENST00000654170.1:n.1109G>A
ENST00000656590.1:c.5056G>A
ENST00000661310.1:c.6074G>A	ENSP00000499589.1:p.Arg2025Gln
ENST00000665483.1:n.121G>A
ENST00000666447.1:n.101G>A
ENST00000666943.1:n.1730G>A
ENST00000350721.8:c.6266G>A	ENSP00000343741.4:p.Arg2089Gln
NM_001184.3:c.6266G>A	NP_001175.2:p.Arg2089Gln
XM_011512924.1:c.6272G>A	XP_011511226.1:p.Arg2091Gln
XM_011512925.1:c.6080G>A	XP_011511227.1:p.Arg2027Gln
XR_924147.1:n.6361G>A
XR_924148.1:n.6361G>A
XR_924149.1:n.6240G>A
NM_001354579.1:c.6074G>A	NP_001341508.1:p.Arg2025Gln
XR_001740179.2:n.6355G>A
XR_001740180.2:n.6409G>A
XR_001740181.2:n.6288G>A
XR_001740182.1:n.6240G>A
XR_002959543.1:n.6465G>A
XR_924148.2:n.6361G>A
NM_001184.4:c.6266G>A MANE Select	NP_001175.2:p.Arg2089Gln
NM_001354579.2:c.6074G>A	NP_001341508.1:p.Arg2025Gln