Canonical Allele Identifier: CA1054350127
Gene: ATR HGNC NCBI

Linked Data

dbSNP Id: rs2034552205

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553454_142553455insTA , CM000665.2:g.142553454_142553455insTA GRCh38
NC_000003.11:g.142272296_142272297insTA , CM000665.1:g.142272296_142272297insTA GRCh37
NC_000003.10:g.143754986_143754987insTA NCBI36
NG_008951.1:g.30373_30374insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2634-56_2634-55insAT MANE Select ENSP00000343741.4:n.2634-56_2634-55insAT
ENST00000515149.3:c.*1408-56_*1408-55insAT ENSP00000425897.3:n.*1408-56_*1408-55insAT
ENST00000653868.1:n.2663-56_2663-55insAT
ENST00000656590.1:c.1424-56_1424-55insAT
ENST00000659195.1:n.5509-56_5509-55insAT
ENST00000661310.1:c.2442-56_2442-55insAT ENSP00000499589.1:n.2442-56_2442-55insAT
ENST00000350721.8:c.2634-56_2634-55insAT ENSP00000343741.4:n.2634-56_2634-55insAT
NM_001184.3:c.2634-56_2634-55insAT NP_001175.2:n.2634-56_2634-55insAT
XM_011512924.1:c.2634-56_2634-55insAT XP_011511226.1:n.2634-56_2634-55insAT
XM_011512925.1:c.2442-56_2442-55insAT XP_011511227.1:n.2442-56_2442-55insAT
XM_011512926.1:c.2634-56_2634-55insAT XP_011511228.1:n.2634-56_2634-55insAT
XM_011512927.1:c.2634-56_2634-55insAT XP_011511229.1:n.2634-56_2634-55insAT
XR_924147.1:n.2723-56_2723-55insAT
XR_924148.1:n.2723-56_2723-55insAT
XR_924149.1:n.2723-56_2723-55insAT
NM_001354579.1:c.2442-56_2442-55insAT NP_001341508.1:n.2442-56_2442-55insAT
XR_001740179.2:n.2723-56_2723-55insAT
XR_001740180.2:n.2723-56_2723-55insAT
XR_001740181.2:n.2723-56_2723-55insAT
XR_001740182.1:n.2723-56_2723-55insAT
XR_002959543.1:n.2723-56_2723-55insAT
XR_924148.2:n.2723-56_2723-55insAT
NM_001184.4:c.2634-56_2634-55insAT MANE Select NP_001175.2:n.2634-56_2634-55insAT
NM_001354579.2:c.2442-56_2442-55insAT NP_001341508.1:n.2442-56_2442-55insAT