Canonical Allele Identifier: CA2668018862
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553774_142553782del , CM000665.2:g.142553774_142553782del GRCh38
NC_000003.11:g.142272616_142272624del , CM000665.1:g.142272616_142272624del GRCh37
NC_000003.10:g.143755306_143755314del NCBI36
NG_008951.1:g.30046_30054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2533-41_2533-33del MANE Select ENSP00000343741.4:n.2533-41_2533-33del
ENST00000515149.3:c.*1307-41_*1307-33del ENSP00000425897.3:n.*1307-41_*1307-33del
ENST00000653868.1:n.2562-41_2562-33del
ENST00000656590.1:c.1323-41_1323-33del
ENST00000659195.1:n.5408-41_5408-33del
ENST00000661310.1:c.2341-41_2341-33del ENSP00000499589.1:n.2341-41_2341-33del
ENST00000350721.8:c.2533-41_2533-33del ENSP00000343741.4:n.2533-41_2533-33del
NM_001184.3:c.2533-41_2533-33del NP_001175.2:n.2533-41_2533-33del
XM_011512924.1:c.2533-41_2533-33del XP_011511226.1:n.2533-41_2533-33del
XM_011512925.1:c.2341-41_2341-33del XP_011511227.1:n.2341-41_2341-33del
XM_011512926.1:c.2533-41_2533-33del XP_011511228.1:n.2533-41_2533-33del
XM_011512927.1:c.2533-41_2533-33del XP_011511229.1:n.2533-41_2533-33del
XR_924147.1:n.2622-41_2622-33del
XR_924148.1:n.2622-41_2622-33del
XR_924149.1:n.2622-41_2622-33del
NM_001354579.1:c.2341-41_2341-33del NP_001341508.1:n.2341-41_2341-33del
XR_001740179.2:n.2622-41_2622-33del
XR_001740180.2:n.2622-41_2622-33del
XR_001740181.2:n.2622-41_2622-33del
XR_001740182.1:n.2622-41_2622-33del
XR_002959543.1:n.2622-41_2622-33del
XR_924148.2:n.2622-41_2622-33del
NM_001184.4:c.2533-41_2533-33del MANE Select NP_001175.2:n.2533-41_2533-33del
NM_001354579.2:c.2341-41_2341-33del NP_001341508.1:n.2341-41_2341-33del