Canonical Allele Identifier: CA436107063

Gene: ATR

Linked Data

• MyVariant Identifiers: chr3:g.142168391A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449549A>C , CM000665.2:g.142449549A>C	GRCh38
NC_000003.11:g.142168391A>C , CM000665.1:g.142168391A>C	GRCh37
NC_000003.10:g.143651081A>C	NCBI36
NG_008951.1:g.134278T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7815T>G MANE Select	ENSP00000343741.4:p.Thr2605=
ENST00000513291.2:n.6524T>G
ENST00000653893.1:n.2673T>G
ENST00000654170.1:n.2658T>G
ENST00000656114.1:n.2901T>G
ENST00000656590.1:c.6742T>G
ENST00000658083.1:n.2995T>G
ENST00000661310.1:c.7623T>G	ENSP00000499589.1:p.Thr2541=
ENST00000665483.1:n.5355T>G
ENST00000666447.1:n.4318T>G
ENST00000666943.1:n.4547T>G
ENST00000350721.8:c.7815T>G	ENSP00000343741.4:p.Thr2605=
ENST00000504521.5:c.404T>G	ENSP00000422553.1:n.404T>G
ENST00000513291.1:c.4879T>G
ENST00000515810.1:c.241T>G	ENSP00000421870.1:n.241T>G
NM_001184.3:c.7815T>G	NP_001175.2:p.Thr2605=
XM_011512924.1:c.7821T>G	XP_011511226.1:p.Thr2607=
XM_011512925.1:c.7629T>G	XP_011511227.1:p.Thr2543=
XR_924147.1:n.10572T>G
XR_924148.1:n.8047T>G
NM_001354579.1:c.7623T>G	NP_001341508.1:p.Thr2541=
XR_001740179.2:n.8041T>G
XR_924148.2:n.8047T>G
NM_001184.4:c.7815T>G MANE Select	NP_001175.2:p.Thr2605=
NM_001354579.2:c.7623T>G	NP_001341508.1:p.Thr2541=