Canonical Allele Identifier: CA1407029317
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553449_142553459delinsCACACACACAT , CM000665.2:g.142553449_142553459delinsCACACACACAT GRCh38
NC_000003.11:g.142272291_142272301delinsCACACACACAT , CM000665.1:g.142272291_142272301delinsCACACACACAT GRCh37
NC_000003.10:g.143754981_143754991delinsCACACACACAT NCBI36
NG_008951.1:g.30368_30378delinsATGTGTGTGTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2634-61_2634-51delinsATGTGTGTGTG MANE Select ENSP00000343741.4:n.2634-61_2634-51delinsATGTGTGTGTG
ENST00000515149.3:c.*1408-61_*1408-51delinsATGTGTGTGTG ENSP00000425897.3:n.*1408-61_*1408-51delinsATGTGTGTGTG
ENST00000653868.1:n.2663-61_2663-51delinsATGTGTGTGTG
ENST00000656590.1:c.1424-61_1424-51delinsATGTGTGTGTG
ENST00000659195.1:n.5509-61_5509-51delinsATGTGTGTGTG
ENST00000661310.1:c.2442-61_2442-51delinsATGTGTGTGTG ENSP00000499589.1:n.2442-61_2442-51delinsATGTGTGTGTG
ENST00000350721.8:c.2634-61_2634-51delinsATGTGTGTGTG ENSP00000343741.4:n.2634-61_2634-51delinsATGTGTGTGTG
NM_001184.3:c.2634-61_2634-51delinsATGTGTGTGTG NP_001175.2:n.2634-61_2634-51delinsATGTGTGTGTG
XM_011512924.1:c.2634-61_2634-51delinsATGTGTGTGTG XP_011511226.1:n.2634-61_2634-51delinsATGTGTGTGTG
XM_011512925.1:c.2442-61_2442-51delinsATGTGTGTGTG XP_011511227.1:n.2442-61_2442-51delinsATGTGTGTGTG
XM_011512926.1:c.2634-61_2634-51delinsATGTGTGTGTG XP_011511228.1:n.2634-61_2634-51delinsATGTGTGTGTG
XM_011512927.1:c.2634-61_2634-51delinsATGTGTGTGTG XP_011511229.1:n.2634-61_2634-51delinsATGTGTGTGTG
XR_924147.1:n.2723-61_2723-51delinsATGTGTGTGTG
XR_924148.1:n.2723-61_2723-51delinsATGTGTGTGTG
XR_924149.1:n.2723-61_2723-51delinsATGTGTGTGTG
NM_001354579.1:c.2442-61_2442-51delinsATGTGTGTGTG NP_001341508.1:n.2442-61_2442-51delinsATGTGTGTGTG
XR_001740179.2:n.2723-61_2723-51delinsATGTGTGTGTG
XR_001740180.2:n.2723-61_2723-51delinsATGTGTGTGTG
XR_001740181.2:n.2723-61_2723-51delinsATGTGTGTGTG
XR_001740182.1:n.2723-61_2723-51delinsATGTGTGTGTG
XR_002959543.1:n.2723-61_2723-51delinsATGTGTGTGTG
XR_924148.2:n.2723-61_2723-51delinsATGTGTGTGTG
NM_001184.4:c.2634-61_2634-51delinsATGTGTGTGTG MANE Select NP_001175.2:n.2634-61_2634-51delinsATGTGTGTGTG
NM_001354579.2:c.2442-61_2442-51delinsATGTGTGTGTG NP_001341508.1:n.2442-61_2442-51delinsATGTGTGTGTG