Canonical Allele Identifier: CA2668039291
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470191_142470193del , CM000665.2:g.142470191_142470193del GRCh38
NC_000003.11:g.142189033_142189035del , CM000665.1:g.142189033_142189035del GRCh37
NC_000003.10:g.143671723_143671725del NCBI36
NG_008951.1:g.113636_113638del

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.6222-8_6222-6del MANE Select ENSP00000343741.4:n.6222-8_6222-6del
ENST00000513291.2:n.1406-8_1406-6del
ENST00000654170.1:n.1065-8_1065-6del
ENST00000656590.1:c.5012-8_5012-6del
ENST00000661310.1:c.6030-8_6030-6del ENSP00000499589.1:n.6030-8_6030-6del
ENST00000665483.1:n.77-8_77-6del
ENST00000666447.1:n.57-8_57-6del
ENST00000666943.1:n.1686-8_1686-6del
ENST00000350721.8:c.6222-8_6222-6del ENSP00000343741.4:n.6222-8_6222-6del
NM_001184.3:c.6222-8_6222-6del NP_001175.2:n.6222-8_6222-6del
XM_011512924.1:c.6228-8_6228-6del XP_011511226.1:n.6228-8_6228-6del
XM_011512925.1:c.6036-8_6036-6del XP_011511227.1:n.6036-8_6036-6del
XR_924147.1:n.6317-8_6317-6del
XR_924148.1:n.6317-8_6317-6del
XR_924149.1:n.6196-8_6196-6del
NM_001354579.1:c.6030-8_6030-6del NP_001341508.1:n.6030-8_6030-6del
XR_001740179.2:n.6311-8_6311-6del
XR_001740180.2:n.6365-8_6365-6del
XR_001740181.2:n.6244-8_6244-6del
XR_001740182.1:n.6196-8_6196-6del
XR_002959543.1:n.6421-8_6421-6del
XR_924148.2:n.6317-8_6317-6del
NM_001184.4:c.6222-8_6222-6del MANE Select NP_001175.2:n.6222-8_6222-6del
NM_001354579.2:c.6030-8_6030-6del NP_001341508.1:n.6030-8_6030-6del