Canonical Allele Identifier: CA1054350135
Gene: ATR HGNC NCBI

Linked Data

dbSNP Id: rs2034552386

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553456_142553457insTA , CM000665.2:g.142553456_142553457insTA GRCh38
NC_000003.11:g.142272298_142272299insTA , CM000665.1:g.142272298_142272299insTA GRCh37
NC_000003.10:g.143754988_143754989insTA NCBI36
NG_008951.1:g.30371_30372insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2634-58_2634-57insAT MANE Select ENSP00000343741.4:n.2634-58_2634-57insAT
ENST00000515149.3:c.*1408-58_*1408-57insAT ENSP00000425897.3:n.*1408-58_*1408-57insAT
ENST00000653868.1:n.2663-58_2663-57insAT
ENST00000656590.1:c.1424-58_1424-57insAT
ENST00000659195.1:n.5509-58_5509-57insAT
ENST00000661310.1:c.2442-58_2442-57insAT ENSP00000499589.1:n.2442-58_2442-57insAT
ENST00000350721.8:c.2634-58_2634-57insAT ENSP00000343741.4:n.2634-58_2634-57insAT
NM_001184.3:c.2634-58_2634-57insAT NP_001175.2:n.2634-58_2634-57insAT
XM_011512924.1:c.2634-58_2634-57insAT XP_011511226.1:n.2634-58_2634-57insAT
XM_011512925.1:c.2442-58_2442-57insAT XP_011511227.1:n.2442-58_2442-57insAT
XM_011512926.1:c.2634-58_2634-57insAT XP_011511228.1:n.2634-58_2634-57insAT
XM_011512927.1:c.2634-58_2634-57insAT XP_011511229.1:n.2634-58_2634-57insAT
XR_924147.1:n.2723-58_2723-57insAT
XR_924148.1:n.2723-58_2723-57insAT
XR_924149.1:n.2723-58_2723-57insAT
NM_001354579.1:c.2442-58_2442-57insAT NP_001341508.1:n.2442-58_2442-57insAT
XR_001740179.2:n.2723-58_2723-57insAT
XR_001740180.2:n.2723-58_2723-57insAT
XR_001740181.2:n.2723-58_2723-57insAT
XR_001740182.1:n.2723-58_2723-57insAT
XR_002959543.1:n.2723-58_2723-57insAT
XR_924148.2:n.2723-58_2723-57insAT
NM_001184.4:c.2634-58_2634-57insAT MANE Select NP_001175.2:n.2634-58_2634-57insAT
NM_001354579.2:c.2442-58_2442-57insAT NP_001341508.1:n.2442-58_2442-57insAT