Canonical Allele Identifier: CA2586973089
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470154_142470155insC , CM000665.2:g.142470154_142470155insC GRCh38
NC_000003.11:g.142188996_142188997insC , CM000665.1:g.142188996_142188997insC GRCh37
NC_000003.10:g.143671686_143671687insC NCBI36
NG_008951.1:g.113672_113673insG

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6250_6251insG MANE Select ENSP00000343741.4:p.Tyr2084Ter
ENST00000513291.2:n.1434_1435insG
ENST00000654170.1:n.1093_1094insG
ENST00000656590.1:c.5040_5041insG
ENST00000661310.1:c.6058_6059insG ENSP00000499589.1:p.Tyr2020Ter
ENST00000665483.1:n.105_106insG
ENST00000666447.1:n.85_86insG
ENST00000666943.1:n.1714_1715insG
ENST00000350721.8:c.6250_6251insG ENSP00000343741.4:p.Tyr2084Ter
NM_001184.3:c.6250_6251insG NP_001175.2:p.Tyr2084Ter
XM_011512924.1:c.6256_6257insG XP_011511226.1:p.Tyr2086Ter
XM_011512925.1:c.6064_6065insG XP_011511227.1:p.Tyr2022Ter
XR_924147.1:n.6345_6346insG
XR_924148.1:n.6345_6346insG
XR_924149.1:n.6224_6225insG
NM_001354579.1:c.6058_6059insG NP_001341508.1:p.Tyr2020Ter
XR_001740179.2:n.6339_6340insG
XR_001740180.2:n.6393_6394insG
XR_001740181.2:n.6272_6273insG
XR_001740182.1:n.6224_6225insG
XR_002959543.1:n.6449_6450insG
XR_924148.2:n.6345_6346insG
NM_001184.4:c.6250_6251insG MANE Select NP_001175.2:p.Tyr2084Ter
NM_001354579.2:c.6058_6059insG NP_001341508.1:p.Tyr2020Ter