Canonical Allele Identifier: CA354796861

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142232391A>C (hg19) ; chr3:g.142513549A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142513549A>C , CM000665.2:g.142513549A>C	GRCh38
NC_000003.11:g.142232391A>C , CM000665.1:g.142232391A>C	GRCh37
NC_000003.10:g.143715081A>C	NCBI36
NG_008951.1:g.70278T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.4593T>G MANE Select	ENSP00000343741.4:p.His1531Gln
ENST00000653868.1:n.4622T>G
ENST00000656590.1:c.3383T>G
ENST00000661310.1:c.4401T>G	ENSP00000499589.1:p.His1467Gln
ENST00000666943.1:n.57T>G
ENST00000350721.8:c.4593T>G	ENSP00000343741.4:p.His1531Gln
NM_001184.3:c.4593T>G	NP_001175.2:p.His1531Gln
XM_011512924.1:c.4599T>G	XP_011511226.1:p.His1533Gln
XM_011512925.1:c.4407T>G	XP_011511227.1:p.His1469Gln
XM_011512926.1:c.4599T>G	XP_011511228.1:p.His1533Gln
XM_011512927.1:c.4599T>G	XP_011511229.1:p.His1533Gln
XR_924147.1:n.4688T>G
XR_924148.1:n.4688T>G
XR_924149.1:n.4688T>G
NM_001354579.1:c.4401T>G	NP_001341508.1:p.His1467Gln
XR_001740179.2:n.4682T>G
XR_001740180.2:n.4688T>G
XR_001740181.2:n.4688T>G
XR_001740182.1:n.4688T>G
XR_002959543.1:n.4688T>G
XR_924148.2:n.4688T>G
NM_001184.4:c.4593T>G MANE Select	NP_001175.2:p.His1531Gln
NM_001354579.2:c.4401T>G	NP_001341508.1:p.His1467Gln