Canonical Allele Identifier: CA436125951

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188938T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470096T>C , CM000665.2:g.142470096T>C	GRCh38
NC_000003.11:g.142188938T>C , CM000665.1:g.142188938T>C	GRCh37
NC_000003.10:g.143671628T>C	NCBI36
NG_008951.1:g.113731A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6309A>G MANE Select	ENSP00000343741.4:p.Glu2103=
ENST00000513291.2:n.1493A>G
ENST00000654170.1:n.1152A>G
ENST00000656590.1:c.5099A>G
ENST00000661310.1:c.6117A>G	ENSP00000499589.1:p.Glu2039=
ENST00000665483.1:n.164A>G
ENST00000666447.1:n.144A>G
ENST00000666943.1:n.1773A>G
ENST00000350721.8:c.6309A>G	ENSP00000343741.4:p.Glu2103=
NM_001184.3:c.6309A>G	NP_001175.2:p.Glu2103=
XM_011512924.1:c.6315A>G	XP_011511226.1:p.Glu2105=
XM_011512925.1:c.6123A>G	XP_011511227.1:p.Glu2041=
XR_924147.1:n.6404A>G
XR_924148.1:n.6404A>G
XR_924149.1:n.6283A>G
NM_001354579.1:c.6117A>G	NP_001341508.1:p.Glu2039=
XR_001740179.2:n.6398A>G
XR_001740180.2:n.6452A>G
XR_001740181.2:n.6331A>G
XR_001740182.1:n.6283A>G
XR_002959543.1:n.6508A>G
XR_924148.2:n.6404A>G
NM_001184.4:c.6309A>G MANE Select	NP_001175.2:p.Glu2103=
NM_001354579.2:c.6117A>G	NP_001341508.1:p.Glu2039=