Canonical Allele Identifier: CA2704280530
Gene: ATR HGNC NCBI

Linked Data

dbSNP Id: rs2108462982

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553416_142553417insC , CM000665.2:g.142553416_142553417insC GRCh38
NC_000003.11:g.142272258_142272259insC , CM000665.1:g.142272258_142272259insC GRCh37
NC_000003.10:g.143754948_143754949insC NCBI36
NG_008951.1:g.30410_30411insG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2634-19_2634-18insG MANE Select ENSP00000343741.4:n.2634-19_2634-18insG
ENST00000515149.3:c.*1408-19_*1408-18insG ENSP00000425897.3:n.*1408-19_*1408-18insG
ENST00000653868.1:n.2663-19_2663-18insG
ENST00000656590.1:c.1424-19_1424-18insG
ENST00000659195.1:n.5509-19_5509-18insG
ENST00000661310.1:c.2442-19_2442-18insG ENSP00000499589.1:n.2442-19_2442-18insG
ENST00000350721.8:c.2634-19_2634-18insG ENSP00000343741.4:n.2634-19_2634-18insG
NM_001184.3:c.2634-19_2634-18insG NP_001175.2:n.2634-19_2634-18insG
XM_011512924.1:c.2634-19_2634-18insG XP_011511226.1:n.2634-19_2634-18insG
XM_011512925.1:c.2442-19_2442-18insG XP_011511227.1:n.2442-19_2442-18insG
XM_011512926.1:c.2634-19_2634-18insG XP_011511228.1:n.2634-19_2634-18insG
XM_011512927.1:c.2634-19_2634-18insG XP_011511229.1:n.2634-19_2634-18insG
XR_924147.1:n.2723-19_2723-18insG
XR_924148.1:n.2723-19_2723-18insG
XR_924149.1:n.2723-19_2723-18insG
NM_001354579.1:c.2442-19_2442-18insG NP_001341508.1:n.2442-19_2442-18insG
XR_001740179.2:n.2723-19_2723-18insG
XR_001740180.2:n.2723-19_2723-18insG
XR_001740181.2:n.2723-19_2723-18insG
XR_001740182.1:n.2723-19_2723-18insG
XR_002959543.1:n.2723-19_2723-18insG
XR_924148.2:n.2723-19_2723-18insG
NM_001184.4:c.2634-19_2634-18insG MANE Select NP_001175.2:n.2634-19_2634-18insG
NM_001354579.2:c.2442-19_2442-18insG NP_001341508.1:n.2442-19_2442-18insG