Canonical Allele Identifier: CA1406991869
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470099A= , CM000665.2:g.142470099A= GRCh38
NC_000003.11:g.142188941A= , CM000665.1:g.142188941A= GRCh37
NC_000003.10:g.143671631A= NCBI36
NG_008951.1:g.113728T=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6306T= MANE Select ENSP00000343741.4:p.Tyr2102=
ENST00000513291.2:n.1490T=
ENST00000654170.1:n.1149T=
ENST00000656590.1:c.5096T=
ENST00000661310.1:c.6114T= ENSP00000499589.1:p.Tyr2038=
ENST00000665483.1:n.161T=
ENST00000666447.1:n.141T=
ENST00000666943.1:n.1770T=
ENST00000350721.8:c.6306T= ENSP00000343741.4:p.Tyr2102=
NM_001184.3:c.6306T= NP_001175.2:p.Tyr2102=
XM_011512924.1:c.6312T= XP_011511226.1:p.Tyr2104=
XM_011512925.1:c.6120T= XP_011511227.1:p.Tyr2040=
XR_924147.1:n.6401T=
XR_924148.1:n.6401T=
XR_924149.1:n.6280T=
NM_001354579.1:c.6114T= NP_001341508.1:p.Tyr2038=
XR_001740179.2:n.6395T=
XR_001740180.2:n.6449T=
XR_001740181.2:n.6328T=
XR_001740182.1:n.6280T=
XR_002959543.1:n.6505T=
XR_924148.2:n.6401T=
NM_001184.4:c.6306T= MANE Select NP_001175.2:p.Tyr2102=
NM_001354579.2:c.6114T= NP_001341508.1:p.Tyr2038=