Canonical Allele Identifier: CA354805804

Gene: ATR

Linked Data

• ClinVar Variation Id: 1752516
• ClinVar RCV Id: RCV002368631
• MyVariant Identifiers: chr3:g.142188981C>G (hg19) ; chr3:g.142470139C>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6266G>C MANE Select	ENSP00000343741.4:p.Arg2089Pro
ENST00000513291.2:n.1450G>C
ENST00000654170.1:n.1109G>C
ENST00000656590.1:c.5056G>C
ENST00000661310.1:c.6074G>C	ENSP00000499589.1:p.Arg2025Pro
ENST00000665483.1:n.121G>C
ENST00000666447.1:n.101G>C
ENST00000666943.1:n.1730G>C
ENST00000350721.8:c.6266G>C	ENSP00000343741.4:p.Arg2089Pro
NM_001184.3:c.6266G>C	NP_001175.2:p.Arg2089Pro
XM_011512924.1:c.6272G>C	XP_011511226.1:p.Arg2091Pro
XM_011512925.1:c.6080G>C	XP_011511227.1:p.Arg2027Pro
XR_924147.1:n.6361G>C
XR_924148.1:n.6361G>C
XR_924149.1:n.6240G>C
NM_001354579.1:c.6074G>C	NP_001341508.1:p.Arg2025Pro
XR_001740179.2:n.6355G>C
XR_001740180.2:n.6409G>C
XR_001740181.2:n.6288G>C
XR_001740182.1:n.6240G>C
XR_002959543.1:n.6465G>C
XR_924148.2:n.6361G>C
NM_001184.4:c.6266G>C MANE Select	NP_001175.2:p.Arg2089Pro
NM_001354579.2:c.6074G>C	NP_001341508.1:p.Arg2025Pro