Canonical Allele Identifier: CA436106543

Gene: ATR

Linked Data

• ClinVar Variation Id: 1607527
• ClinVar RCV Id: RCV002144638
• dbSNP Id: rs2108375558
• MyVariant Identifiers: chr3:g.142232478A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513636A>T , CM000665.2:g.142513636A>T	GRCh38
NC_000003.11:g.142232478A>T , CM000665.1:g.142232478A>T	GRCh37
NC_000003.10:g.143715168A>T	NCBI36
NG_008951.1:g.70191T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4506T>A MANE Select	ENSP00000343741.4:p.Val1502=
ENST00000653868.1:n.4535T>A
ENST00000656590.1:c.3296T>A
ENST00000661310.1:c.4314T>A	ENSP00000499589.1:p.Val1438=
ENST00000350721.8:c.4506T>A	ENSP00000343741.4:p.Val1502=
NM_001184.3:c.4506T>A	NP_001175.2:p.Val1502=
XM_011512924.1:c.4512T>A	XP_011511226.1:p.Val1504=
XM_011512925.1:c.4320T>A	XP_011511227.1:p.Val1440=
XM_011512926.1:c.4512T>A	XP_011511228.1:p.Val1504=
XM_011512927.1:c.4512T>A	XP_011511229.1:p.Val1504=
XR_924147.1:n.4601T>A
XR_924148.1:n.4601T>A
XR_924149.1:n.4601T>A
NM_001354579.1:c.4314T>A	NP_001341508.1:p.Val1438=
XR_001740179.2:n.4595T>A
XR_001740180.2:n.4601T>A
XR_001740181.2:n.4601T>A
XR_001740182.1:n.4601T>A
XR_002959543.1:n.4601T>A
XR_924148.2:n.4601T>A
NM_001184.4:c.4506T>A MANE Select	NP_001175.2:p.Val1502=
NM_001354579.2:c.4314T>A	NP_001341508.1:p.Val1438=