Canonical Allele Identifier: CA1406991868
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470097T= , CM000665.2:g.142470097T= GRCh38
NC_000003.11:g.142188939T= , CM000665.1:g.142188939T= GRCh37
NC_000003.10:g.143671629T= NCBI36
NG_008951.1:g.113730A=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6308A= MANE Select ENSP00000343741.4:p.Glu2103=
ENST00000513291.2:n.1492A=
ENST00000654170.1:n.1151A=
ENST00000656590.1:c.5098A=
ENST00000661310.1:c.6116A= ENSP00000499589.1:p.Glu2039=
ENST00000665483.1:n.163A=
ENST00000666447.1:n.143A=
ENST00000666943.1:n.1772A=
ENST00000350721.8:c.6308A= ENSP00000343741.4:p.Glu2103=
NM_001184.3:c.6308A= NP_001175.2:p.Glu2103=
XM_011512924.1:c.6314A= XP_011511226.1:p.Glu2105=
XM_011512925.1:c.6122A= XP_011511227.1:p.Glu2041=
XR_924147.1:n.6403A=
XR_924148.1:n.6403A=
XR_924149.1:n.6282A=
NM_001354579.1:c.6116A= NP_001341508.1:p.Glu2039=
XR_001740179.2:n.6397A=
XR_001740180.2:n.6451A=
XR_001740181.2:n.6330A=
XR_001740182.1:n.6282A=
XR_002959543.1:n.6507A=
XR_924148.2:n.6403A=
NM_001184.4:c.6308A= MANE Select NP_001175.2:p.Glu2103=
NM_001354579.2:c.6116A= NP_001341508.1:p.Glu2039=