Canonical Allele Identifier: CA1407011979
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142515446A= , CM000665.2:g.142515446A= GRCh38
NC_000003.11:g.142234288A= , CM000665.1:g.142234288A= GRCh37
NC_000003.10:g.143716978A= NCBI36
NG_008951.1:g.68381T=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.4452T= MANE Select ENSP00000343741.4:p.Gly1484=
ENST00000653868.1:n.4481T=
ENST00000656590.1:c.3242T=
ENST00000661310.1:c.4260T= ENSP00000499589.1:p.Gly1420=
ENST00000350721.8:c.4452T= ENSP00000343741.4:p.Gly1484=
NM_001184.3:c.4452T= NP_001175.2:p.Gly1484=
XM_011512924.1:c.4458T= XP_011511226.1:p.Gly1486=
XM_011512925.1:c.4266T= XP_011511227.1:p.Gly1422=
XM_011512926.1:c.4458T= XP_011511228.1:p.Gly1486=
XM_011512927.1:c.4458T= XP_011511229.1:p.Gly1486=
XR_924147.1:n.4547T=
XR_924148.1:n.4547T=
XR_924149.1:n.4547T=
NM_001354579.1:c.4260T= NP_001341508.1:p.Gly1420=
XR_001740179.2:n.4541T=
XR_001740180.2:n.4547T=
XR_001740181.2:n.4547T=
XR_001740182.1:n.4547T=
XR_002959543.1:n.4547T=
XR_924148.2:n.4547T=
NM_001184.4:c.4452T= MANE Select NP_001175.2:p.Gly1484=
NM_001354579.2:c.4260T= NP_001341508.1:p.Gly1420=