Canonical Allele Identifier: CA436125976

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188980T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470138T>C , CM000665.2:g.142470138T>C	GRCh38
NC_000003.11:g.142188980T>C , CM000665.1:g.142188980T>C	GRCh37
NC_000003.10:g.143671670T>C	NCBI36
NG_008951.1:g.113689A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6267A>G MANE Select	ENSP00000343741.4:p.Arg2089=
ENST00000513291.2:n.1451A>G
ENST00000654170.1:n.1110A>G
ENST00000656590.1:c.5057A>G
ENST00000661310.1:c.6075A>G	ENSP00000499589.1:p.Arg2025=
ENST00000665483.1:n.122A>G
ENST00000666447.1:n.102A>G
ENST00000666943.1:n.1731A>G
ENST00000350721.8:c.6267A>G	ENSP00000343741.4:p.Arg2089=
NM_001184.3:c.6267A>G	NP_001175.2:p.Arg2089=
XM_011512924.1:c.6273A>G	XP_011511226.1:p.Arg2091=
XM_011512925.1:c.6081A>G	XP_011511227.1:p.Arg2027=
XR_924147.1:n.6362A>G
XR_924148.1:n.6362A>G
XR_924149.1:n.6241A>G
NM_001354579.1:c.6075A>G	NP_001341508.1:p.Arg2025=
XR_001740179.2:n.6356A>G
XR_001740180.2:n.6410A>G
XR_001740181.2:n.6289A>G
XR_001740182.1:n.6241A>G
XR_002959543.1:n.6466A>G
XR_924148.2:n.6362A>G
NM_001184.4:c.6267A>G MANE Select	NP_001175.2:p.Arg2089=
NM_001354579.2:c.6075A>G	NP_001341508.1:p.Arg2025=