Canonical Allele Identifier: CA2704280916

Gene: ATR

Linked Data

• dbSNP Id: rs2108463262

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553457_142553458insCC , CM000665.2:g.142553457_142553458insCC	GRCh38
NC_000003.11:g.142272299_142272300insCC , CM000665.1:g.142272299_142272300insCC	GRCh37
NC_000003.10:g.143754989_143754990insCC	NCBI36
NG_008951.1:g.30370_30371insGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2634-59_2634-58insGG MANE Select	ENSP00000343741.4:n.2634-59_2634-58insGG
ENST00000515149.3:c.*1408-59_*1408-58insGG	ENSP00000425897.3:n.*1408-59_*1408-58insGG
ENST00000653868.1:n.2663-59_2663-58insGG
ENST00000656590.1:c.1424-59_1424-58insGG
ENST00000659195.1:n.5509-59_5509-58insGG
ENST00000661310.1:c.2442-59_2442-58insGG	ENSP00000499589.1:n.2442-59_2442-58insGG
ENST00000350721.8:c.2634-59_2634-58insGG	ENSP00000343741.4:n.2634-59_2634-58insGG
NM_001184.3:c.2634-59_2634-58insGG	NP_001175.2:n.2634-59_2634-58insGG
XM_011512924.1:c.2634-59_2634-58insGG	XP_011511226.1:n.2634-59_2634-58insGG
XM_011512925.1:c.2442-59_2442-58insGG	XP_011511227.1:n.2442-59_2442-58insGG
XM_011512926.1:c.2634-59_2634-58insGG	XP_011511228.1:n.2634-59_2634-58insGG
XM_011512927.1:c.2634-59_2634-58insGG	XP_011511229.1:n.2634-59_2634-58insGG
XR_924147.1:n.2723-59_2723-58insGG
XR_924148.1:n.2723-59_2723-58insGG
XR_924149.1:n.2723-59_2723-58insGG
NM_001354579.1:c.2442-59_2442-58insGG	NP_001341508.1:n.2442-59_2442-58insGG
XR_001740179.2:n.2723-59_2723-58insGG
XR_001740180.2:n.2723-59_2723-58insGG
XR_001740181.2:n.2723-59_2723-58insGG
XR_001740182.1:n.2723-59_2723-58insGG
XR_002959543.1:n.2723-59_2723-58insGG
XR_924148.2:n.2723-59_2723-58insGG
NM_001184.4:c.2634-59_2634-58insGG MANE Select	NP_001175.2:n.2634-59_2634-58insGG
NM_001354579.2:c.2442-59_2442-58insGG	NP_001341508.1:n.2442-59_2442-58insGG