Canonical Allele Identifier: CA436125958

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142188950T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470108T>G , CM000665.2:g.142470108T>G	GRCh38
NC_000003.11:g.142188950T>G , CM000665.1:g.142188950T>G	GRCh37
NC_000003.10:g.143671640T>G	NCBI36
NG_008951.1:g.113719A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6297A>C MANE Select	ENSP00000343741.4:p.Thr2099=
ENST00000513291.2:n.1481A>C
ENST00000654170.1:n.1140A>C
ENST00000656590.1:c.5087A>C
ENST00000661310.1:c.6105A>C	ENSP00000499589.1:p.Thr2035=
ENST00000665483.1:n.152A>C
ENST00000666447.1:n.132A>C
ENST00000666943.1:n.1761A>C
ENST00000350721.8:c.6297A>C	ENSP00000343741.4:p.Thr2099=
NM_001184.3:c.6297A>C	NP_001175.2:p.Thr2099=
XM_011512924.1:c.6303A>C	XP_011511226.1:p.Thr2101=
XM_011512925.1:c.6111A>C	XP_011511227.1:p.Thr2037=
XR_924147.1:n.6392A>C
XR_924148.1:n.6392A>C
XR_924149.1:n.6271A>C
NM_001354579.1:c.6105A>C	NP_001341508.1:p.Thr2035=
XR_001740179.2:n.6386A>C
XR_001740180.2:n.6440A>C
XR_001740181.2:n.6319A>C
XR_001740182.1:n.6271A>C
XR_002959543.1:n.6496A>C
XR_924148.2:n.6392A>C
NM_001184.4:c.6297A>C MANE Select	NP_001175.2:p.Thr2099=
NM_001354579.2:c.6105A>C	NP_001341508.1:p.Thr2035=