Canonical Allele Identifier: CA1407011046
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513508T= , CM000665.2:g.142513508T= GRCh38
NC_000003.11:g.142232350T= , CM000665.1:g.142232350T= GRCh37
NC_000003.10:g.143715040T= NCBI36
NG_008951.1:g.70319A=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.4634A= MANE Select ENSP00000343741.4:p.Gln1545=
ENST00000653868.1:n.4663A=
ENST00000656590.1:c.3424A=
ENST00000661310.1:c.4442A= ENSP00000499589.1:p.Gln1481=
ENST00000666943.1:n.98A=
ENST00000350721.8:c.4634A= ENSP00000343741.4:p.Gln1545=
NM_001184.3:c.4634A= NP_001175.2:p.Gln1545=
XM_011512924.1:c.4640A= XP_011511226.1:p.Gln1547=
XM_011512925.1:c.4448A= XP_011511227.1:p.Gln1483=
XM_011512926.1:c.4640A= XP_011511228.1:p.Gln1547=
XM_011512927.1:c.4640A= XP_011511229.1:p.Gln1547=
XR_924147.1:n.4729A=
XR_924148.1:n.4729A=
XR_924149.1:n.4729A=
NM_001354579.1:c.4442A= NP_001341508.1:p.Gln1481=
XR_001740179.2:n.4723A=
XR_001740180.2:n.4729A=
XR_001740181.2:n.4729A=
XR_001740182.1:n.4729A=
XR_002959543.1:n.4729A=
XR_924148.2:n.4729A=
NM_001184.4:c.4634A= MANE Select NP_001175.2:p.Gln1545=
NM_001354579.2:c.4442A= NP_001341508.1:p.Gln1481=