Canonical Allele Identifier: CA1407029532
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553649T= , CM000665.2:g.142553649T= GRCh38
NC_000003.11:g.142272491T= , CM000665.1:g.142272491T= GRCh37
NC_000003.10:g.143755181T= NCBI36
NG_008951.1:g.30178A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2624A= MANE Select ENSP00000343741.4:p.Asp875=
ENST00000515149.3:c.*1398A= ENSP00000425897.3:n.*1398A=
ENST00000653868.1:n.2653A=
ENST00000656590.1:c.1414A=
ENST00000659195.1:n.5499A=
ENST00000661310.1:c.2432A= ENSP00000499589.1:p.Asp811=
ENST00000350721.8:c.2624A= ENSP00000343741.4:p.Asp875=
NM_001184.3:c.2624A= NP_001175.2:p.Asp875=
XM_011512924.1:c.2624A= XP_011511226.1:p.Asp875=
XM_011512925.1:c.2432A= XP_011511227.1:p.Asp811=
XM_011512926.1:c.2624A= XP_011511228.1:p.Asp875=
XM_011512927.1:c.2624A= XP_011511229.1:p.Asp875=
XR_924147.1:n.2713A=
XR_924148.1:n.2713A=
XR_924149.1:n.2713A=
NM_001354579.1:c.2432A= NP_001341508.1:p.Asp811=
XR_001740179.2:n.2713A=
XR_001740180.2:n.2713A=
XR_001740181.2:n.2713A=
XR_001740182.1:n.2713A=
XR_002959543.1:n.2713A=
XR_924148.2:n.2713A=
NM_001184.4:c.2624A= MANE Select NP_001175.2:p.Asp875=
NM_001354579.2:c.2432A= NP_001341508.1:p.Asp811=