Canonical Allele Identifier: CA436172157

Gene: ATR

Linked Data

• ClinVar Variation Id: 2453579
• ClinVar RCV Id: RCV003187714
• MyVariant Identifiers: chr3:g.142281574T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562732T>G , CM000665.2:g.142562732T>G	GRCh38
NC_000003.11:g.142281574T>G , CM000665.1:g.142281574T>G	GRCh37
NC_000003.10:g.143764264T>G	NCBI36
NG_008951.1:g.21095A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.670A>C MANE Select	ENSP00000343741.4:p.Arg224=
ENST00000515149.3:c.293-1311A>C	ENSP00000425897.3:n.293-1311A>C
ENST00000653868.1:n.699A>C
ENST00000657914.1:n.3028A>C
ENST00000659195.1:n.2735A>C
ENST00000661310.1:c.670A>C	ENSP00000499589.1:p.Arg224=
ENST00000350721.8:c.670A>C	ENSP00000343741.4:p.Arg224=
ENST00000507148.1:c.293-384A>C	ENSP00000426595.1:n.293-384A>C
NM_001184.3:c.670A>C	NP_001175.2:p.Arg224=
XM_011512924.1:c.670A>C	XP_011511226.1:p.Arg224=
XM_011512925.1:c.670A>C	XP_011511227.1:p.Arg224=
XM_011512926.1:c.670A>C	XP_011511228.1:p.Arg224=
XM_011512927.1:c.670A>C	XP_011511229.1:p.Arg224=
XR_924147.1:n.759A>C
XR_924148.1:n.759A>C
XR_924149.1:n.759A>C
NM_001354579.1:c.670A>C	NP_001341508.1:p.Arg224=
XR_001740179.2:n.759A>C
XR_001740180.2:n.759A>C
XR_001740181.2:n.759A>C
XR_001740182.1:n.759A>C
XR_002959543.1:n.759A>C
XR_924148.2:n.759A>C
NM_001184.4:c.670A>C MANE Select	NP_001175.2:p.Arg224=
NM_001354579.2:c.670A>C	NP_001341508.1:p.Arg224=