Canonical Allele Identifier: CA1407011174
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513842_142513844delinsCAT , CM000665.2:g.142513842_142513844delinsCAT GRCh38
NC_000003.11:g.142232684_142232686delinsCAT , CM000665.1:g.142232684_142232686delinsCAT GRCh37
NC_000003.10:g.143715374_143715376delinsCAT NCBI36
NG_008951.1:g.69983_69985delinsATG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.4504-206_4504-204delinsATG MANE Select ENSP00000343741.4:n.4504-206_4504-204delinsATG
ENST00000653868.1:n.4533-206_4533-204delinsATG
ENST00000656590.1:c.3294-206_3294-204delinsATG
ENST00000661310.1:c.4312-206_4312-204delinsATG ENSP00000499589.1:n.4312-206_4312-204delinsATG
ENST00000350721.8:c.4504-206_4504-204delinsATG ENSP00000343741.4:n.4504-206_4504-204delinsATG
NM_001184.3:c.4504-206_4504-204delinsATG NP_001175.2:n.4504-206_4504-204delinsATG
XM_011512924.1:c.4510-206_4510-204delinsATG XP_011511226.1:n.4510-206_4510-204delinsATG
XM_011512925.1:c.4318-206_4318-204delinsATG XP_011511227.1:n.4318-206_4318-204delinsATG
XM_011512926.1:c.4510-206_4510-204delinsATG XP_011511228.1:n.4510-206_4510-204delinsATG
XM_011512927.1:c.4510-206_4510-204delinsATG XP_011511229.1:n.4510-206_4510-204delinsATG
XR_924147.1:n.4599-206_4599-204delinsATG
XR_924148.1:n.4599-206_4599-204delinsATG
XR_924149.1:n.4599-206_4599-204delinsATG
NM_001354579.1:c.4312-206_4312-204delinsATG NP_001341508.1:n.4312-206_4312-204delinsATG
XR_001740179.2:n.4593-206_4593-204delinsATG
XR_001740180.2:n.4599-206_4599-204delinsATG
XR_001740181.2:n.4599-206_4599-204delinsATG
XR_001740182.1:n.4599-206_4599-204delinsATG
XR_002959543.1:n.4599-206_4599-204delinsATG
XR_924148.2:n.4599-206_4599-204delinsATG
NM_001184.4:c.4504-206_4504-204delinsATG MANE Select NP_001175.2:n.4504-206_4504-204delinsATG
NM_001354579.2:c.4312-206_4312-204delinsATG NP_001341508.1:n.4312-206_4312-204delinsATG