Canonical Allele Identifier: CA354793981
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142449596T>G , CM000665.2:g.142449596T>G GRCh38
NC_000003.11:g.142168438T>G , CM000665.1:g.142168438T>G GRCh37
NC_000003.10:g.143651128T>G NCBI36
NG_008951.1:g.134231A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.7768A>C MANE Select ENSP00000343741.4:p.Thr2590Pro
ENST00000513291.2:n.6477A>C
ENST00000653893.1:n.2626A>C
ENST00000654170.1:n.2611A>C
ENST00000656114.1:n.2854A>C
ENST00000656590.1:c.6695A>C
ENST00000658083.1:n.2948A>C
ENST00000661310.1:c.7576A>C ENSP00000499589.1:p.Thr2526Pro
ENST00000665483.1:n.5308A>C
ENST00000666447.1:n.4271A>C
ENST00000666943.1:n.4500A>C
ENST00000350721.8:c.7768A>C ENSP00000343741.4:p.Thr2590Pro
ENST00000504521.5:c.357A>C ENSP00000422553.1:n.357A>C
ENST00000513291.1:c.4832A>C
ENST00000515810.1:c.194A>C ENSP00000421870.1:n.194A>C
NM_001184.3:c.7768A>C NP_001175.2:p.Thr2590Pro
XM_011512924.1:c.7774A>C XP_011511226.1:p.Thr2592Pro
XM_011512925.1:c.7582A>C XP_011511227.1:p.Thr2528Pro
XR_924147.1:n.10525A>C
XR_924148.1:n.8000A>C
NM_001354579.1:c.7576A>C NP_001341508.1:p.Thr2526Pro
XR_001740179.2:n.7994A>C
XR_924148.2:n.8000A>C
NM_001184.4:c.7768A>C MANE Select NP_001175.2:p.Thr2590Pro
NM_001354579.2:c.7576A>C NP_001341508.1:p.Thr2526Pro