Canonical Allele Identifier: CA1407029546
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553664A= , CM000665.2:g.142553664A= GRCh38
NC_000003.11:g.142272506A= , CM000665.1:g.142272506A= GRCh37
NC_000003.10:g.143755196A= NCBI36
NG_008951.1:g.30163T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2609T= MANE Select ENSP00000343741.4:p.Ile870=
ENST00000515149.3:c.*1383T= ENSP00000425897.3:n.*1383T=
ENST00000653868.1:n.2638T=
ENST00000656590.1:c.1399T=
ENST00000659195.1:n.5484T=
ENST00000661310.1:c.2417T= ENSP00000499589.1:p.Ile806=
ENST00000350721.8:c.2609T= ENSP00000343741.4:p.Ile870=
NM_001184.3:c.2609T= NP_001175.2:p.Ile870=
XM_011512924.1:c.2609T= XP_011511226.1:p.Ile870=
XM_011512925.1:c.2417T= XP_011511227.1:p.Ile806=
XM_011512926.1:c.2609T= XP_011511228.1:p.Ile870=
XM_011512927.1:c.2609T= XP_011511229.1:p.Ile870=
XR_924147.1:n.2698T=
XR_924148.1:n.2698T=
XR_924149.1:n.2698T=
NM_001354579.1:c.2417T= NP_001341508.1:p.Ile806=
XR_001740179.2:n.2698T=
XR_001740180.2:n.2698T=
XR_001740181.2:n.2698T=
XR_001740182.1:n.2698T=
XR_002959543.1:n.2698T=
XR_924148.2:n.2698T=
NM_001184.4:c.2609T= MANE Select NP_001175.2:p.Ile870=
NM_001354579.2:c.2417T= NP_001341508.1:p.Ile806=