Canonical Allele Identifier: CA2523259327
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470449del , CM000665.2:g.142470449del GRCh38
NC_000003.11:g.142189291del , CM000665.1:g.142189291del GRCh37
NC_000003.10:g.143671981del NCBI36
NG_008951.1:g.113380del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.6222-264del MANE Select ENSP00000343741.4:n.6222-264del
ENST00000513291.2:n.1406-264del
ENST00000654170.1:n.1065-264del
ENST00000656590.1:c.5012-264del
ENST00000661310.1:c.6030-264del ENSP00000499589.1:n.6030-264del
ENST00000665483.1:n.77-264del
ENST00000666447.1:n.57-264del
ENST00000666943.1:n.1686-264del
ENST00000350721.8:c.6222-264del ENSP00000343741.4:n.6222-264del
NM_001184.3:c.6222-264del NP_001175.2:n.6222-264del
XM_011512924.1:c.6228-264del XP_011511226.1:n.6228-264del
XM_011512925.1:c.6036-264del XP_011511227.1:n.6036-264del
XR_924147.1:n.6317-264del
XR_924148.1:n.6317-264del
XR_924149.1:n.6196-264del
NM_001354579.1:c.6030-264del NP_001341508.1:n.6030-264del
XR_001740179.2:n.6311-264del
XR_001740180.2:n.6365-264del
XR_001740181.2:n.6244-264del
XR_001740182.1:n.6196-264del
XR_002959543.1:n.6421-264del
XR_924148.2:n.6317-264del
NM_001184.4:c.6222-264del MANE Select NP_001175.2:n.6222-264del
NM_001354579.2:c.6030-264del NP_001341508.1:n.6030-264del