Canonical Allele Identifier: CA645518355
Gene: ATR HGNC NCBI

Linked Data

COSMIC: COSM53543

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470126_142470127del , CM000665.2:g.142470126_142470127del GRCh38
NC_000003.11:g.142188968_142188969del , CM000665.1:g.142188968_142188969del GRCh37
NC_000003.10:g.143671658_143671659del NCBI36
NG_008951.1:g.113701_113702del

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6279_6280del MANE Select ENSP00000343741.4:p.Trp2094AlafsTer2
ENST00000513291.2:n.1463_1464del
ENST00000654170.1:n.1122_1123del
ENST00000656590.1:c.5069_5070del
ENST00000661310.1:c.6087_6088del ENSP00000499589.1:p.Trp2030AlafsTer2
ENST00000665483.1:n.134_135del
ENST00000666447.1:n.114_115del
ENST00000666943.1:n.1743_1744del
ENST00000350721.8:c.6279_6280del ENSP00000343741.4:p.Trp2094AlafsTer2
NM_001184.3:c.6279_6280del NP_001175.2:p.Trp2094AlafsTer2
XM_011512924.1:c.6285_6286del XP_011511226.1:p.Trp2096AlafsTer2
XM_011512925.1:c.6093_6094del XP_011511227.1:p.Trp2032AlafsTer2
XR_924147.1:n.6374_6375del
XR_924148.1:n.6374_6375del
XR_924149.1:n.6253_6254del
NM_001354579.1:c.6087_6088del NP_001341508.1:p.Trp2030AlafsTer2
XR_001740179.2:n.6368_6369del
XR_001740180.2:n.6422_6423del
XR_001740181.2:n.6301_6302del
XR_001740182.1:n.6253_6254del
XR_002959543.1:n.6478_6479del
XR_924148.2:n.6374_6375del
NM_001184.4:c.6279_6280del MANE Select NP_001175.2:p.Trp2094AlafsTer2
NM_001354579.2:c.6087_6088del NP_001341508.1:p.Trp2030AlafsTer2