Canonical Allele Identifier: CA1407029332

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553457_142553459delinsCAT , CM000665.2:g.142553457_142553459delinsCAT	GRCh38
NC_000003.11:g.142272299_142272301delinsCAT , CM000665.1:g.142272299_142272301delinsCAT	GRCh37
NC_000003.10:g.143754989_143754991delinsCAT	NCBI36
NG_008951.1:g.30368_30370delinsATG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2634-61_2634-59delinsATG MANE Select	ENSP00000343741.4:n.2634-61_2634-59delinsATG
ENST00000515149.3:c.*1408-61_*1408-59delinsATG	ENSP00000425897.3:n.*1408-61_*1408-59delinsATG
ENST00000653868.1:n.2663-61_2663-59delinsATG
ENST00000656590.1:c.1424-61_1424-59delinsATG
ENST00000659195.1:n.5509-61_5509-59delinsATG
ENST00000661310.1:c.2442-61_2442-59delinsATG	ENSP00000499589.1:n.2442-61_2442-59delinsATG
ENST00000350721.8:c.2634-61_2634-59delinsATG	ENSP00000343741.4:n.2634-61_2634-59delinsATG
NM_001184.3:c.2634-61_2634-59delinsATG	NP_001175.2:n.2634-61_2634-59delinsATG
XM_011512924.1:c.2634-61_2634-59delinsATG	XP_011511226.1:n.2634-61_2634-59delinsATG
XM_011512925.1:c.2442-61_2442-59delinsATG	XP_011511227.1:n.2442-61_2442-59delinsATG
XM_011512926.1:c.2634-61_2634-59delinsATG	XP_011511228.1:n.2634-61_2634-59delinsATG
XM_011512927.1:c.2634-61_2634-59delinsATG	XP_011511229.1:n.2634-61_2634-59delinsATG
XR_924147.1:n.2723-61_2723-59delinsATG
XR_924148.1:n.2723-61_2723-59delinsATG
XR_924149.1:n.2723-61_2723-59delinsATG
NM_001354579.1:c.2442-61_2442-59delinsATG	NP_001341508.1:n.2442-61_2442-59delinsATG
XR_001740179.2:n.2723-61_2723-59delinsATG
XR_001740180.2:n.2723-61_2723-59delinsATG
XR_001740181.2:n.2723-61_2723-59delinsATG
XR_001740182.1:n.2723-61_2723-59delinsATG
XR_002959543.1:n.2723-61_2723-59delinsATG
XR_924148.2:n.2723-61_2723-59delinsATG
NM_001184.4:c.2634-61_2634-59delinsATG MANE Select	NP_001175.2:n.2634-61_2634-59delinsATG
NM_001354579.2:c.2442-61_2442-59delinsATG	NP_001341508.1:n.2442-61_2442-59delinsATG