Canonical Allele Identifier: CA354824088

Gene: ATR

Linked Data

• ClinVar Variation Id: 2916681
• ClinVar RCV Id: RCV003740478 ; RCV004374332
• dbSNP Id: rs1320148122
• gnomAD v4: 3-142562405-C-T
• MyVariant Identifiers: chr3:g.142281247C>T (hg19) ; chr3:g.142562405C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562405C>T , CM000665.2:g.142562405C>T	GRCh38
NC_000003.11:g.142281247C>T , CM000665.1:g.142281247C>T	GRCh37
NC_000003.10:g.143763937C>T	NCBI36
NG_008951.1:g.21422G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.997G>A MANE Select	ENSP00000343741.4:p.Val333Met
ENST00000515149.3:c.293-984G>A	ENSP00000425897.3:n.293-984G>A
ENST00000653868.1:n.1026G>A
ENST00000657914.1:n.3355G>A
ENST00000659195.1:n.3062G>A
ENST00000661310.1:c.997G>A	ENSP00000499589.1:p.Val333Met
ENST00000350721.8:c.997G>A	ENSP00000343741.4:p.Val333Met
ENST00000507148.1:c.293-57G>A	ENSP00000426595.1:n.293-57G>A
ENST00000515149.2:c.40G>A	ENSP00000425897.2:p.Val14Met
NM_001184.3:c.997G>A	NP_001175.2:p.Val333Met
XM_011512924.1:c.997G>A	XP_011511226.1:p.Val333Met
XM_011512925.1:c.997G>A	XP_011511227.1:p.Val333Met
XM_011512926.1:c.997G>A	XP_011511228.1:p.Val333Met
XM_011512927.1:c.997G>A	XP_011511229.1:p.Val333Met
XR_924147.1:n.1086G>A
XR_924148.1:n.1086G>A
XR_924149.1:n.1086G>A
NM_001354579.1:c.997G>A	NP_001341508.1:p.Val333Met
XR_001740179.2:n.1086G>A
XR_001740180.2:n.1086G>A
XR_001740181.2:n.1086G>A
XR_001740182.1:n.1086G>A
XR_002959543.1:n.1086G>A
XR_924148.2:n.1086G>A
NM_001184.4:c.997G>A MANE Select	NP_001175.2:p.Val333Met
NM_001354579.2:c.997G>A	NP_001341508.1:p.Val333Met