Canonical Allele Identifier: CA2668039276
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470075_142470076del , CM000665.2:g.142470075_142470076del GRCh38
NC_000003.11:g.142188917_142188918del , CM000665.1:g.142188917_142188918del GRCh37
NC_000003.10:g.143671607_143671608del NCBI36
NG_008951.1:g.113751_113752del

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6319+10_6319+11del MANE Select ENSP00000343741.4:n.6319+10_6319+11del
ENST00000513291.2:n.1503+10_1503+11del
ENST00000654170.1:n.1162+10_1162+11del
ENST00000656590.1:c.5109+10_5109+11del
ENST00000661310.1:c.6127+10_6127+11del ENSP00000499589.1:n.6127+10_6127+11del
ENST00000665483.1:n.174+10_174+11del
ENST00000666447.1:n.154+10_154+11del
ENST00000666943.1:n.1783+10_1783+11del
ENST00000350721.8:c.6319+10_6319+11del ENSP00000343741.4:n.6319+10_6319+11del
NM_001184.3:c.6319+10_6319+11del NP_001175.2:n.6319+10_6319+11del
XM_011512924.1:c.6325+10_6325+11del XP_011511226.1:n.6325+10_6325+11del
XM_011512925.1:c.6133+10_6133+11del XP_011511227.1:n.6133+10_6133+11del
XR_924147.1:n.6414+10_6414+11del
XR_924148.1:n.6414+10_6414+11del
XR_924149.1:n.6293+10_6293+11del
NM_001354579.1:c.6127+10_6127+11del NP_001341508.1:n.6127+10_6127+11del
XR_001740179.2:n.6408+10_6408+11del
XR_001740180.2:n.6462+10_6462+11del
XR_001740181.2:n.6341+10_6341+11del
XR_001740182.1:n.6293+10_6293+11del
XR_002959543.1:n.6518+10_6518+11del
XR_924148.2:n.6414+10_6414+11del
NM_001184.4:c.6319+10_6319+11del MANE Select NP_001175.2:n.6319+10_6319+11del
NM_001354579.2:c.6127+10_6127+11del NP_001341508.1:n.6127+10_6127+11del