Canonical Allele Identifier: CA354805810

Gene: ATR

Linked Data

• dbSNP Id: rs1158115459
• MyVariant Identifiers: chr3:g.142188982G>C (hg19) ; chr3:g.142470140G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470140G>C , CM000665.2:g.142470140G>C	GRCh38
NC_000003.11:g.142188982G>C , CM000665.1:g.142188982G>C	GRCh37
NC_000003.10:g.143671672G>C	NCBI36
NG_008951.1:g.113687C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6265C>G MANE Select	ENSP00000343741.4:p.Arg2089Gly
ENST00000513291.2:n.1449C>G
ENST00000654170.1:n.1108C>G
ENST00000656590.1:c.5055C>G
ENST00000661310.1:c.6073C>G	ENSP00000499589.1:p.Arg2025Gly
ENST00000665483.1:n.120C>G
ENST00000666447.1:n.100C>G
ENST00000666943.1:n.1729C>G
ENST00000350721.8:c.6265C>G	ENSP00000343741.4:p.Arg2089Gly
NM_001184.3:c.6265C>G	NP_001175.2:p.Arg2089Gly
XM_011512924.1:c.6271C>G	XP_011511226.1:p.Arg2091Gly
XM_011512925.1:c.6079C>G	XP_011511227.1:p.Arg2027Gly
XR_924147.1:n.6360C>G
XR_924148.1:n.6360C>G
XR_924149.1:n.6239C>G
NM_001354579.1:c.6073C>G	NP_001341508.1:p.Arg2025Gly
XR_001740179.2:n.6354C>G
XR_001740180.2:n.6408C>G
XR_001740181.2:n.6287C>G
XR_001740182.1:n.6239C>G
XR_002959543.1:n.6464C>G
XR_924148.2:n.6360C>G
NM_001184.4:c.6265C>G MANE Select	NP_001175.2:p.Arg2089Gly
NM_001354579.2:c.6073C>G	NP_001341508.1:p.Arg2025Gly