Canonical Allele Identifier: CA354793987
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142449599T>G , CM000665.2:g.142449599T>G GRCh38
NC_000003.11:g.142168441T>G , CM000665.1:g.142168441T>G GRCh37
NC_000003.10:g.143651131T>G NCBI36
NG_008951.1:g.134228A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.7765A>C MANE Select ENSP00000343741.4:p.Lys2589Gln
ENST00000513291.2:n.6474A>C
ENST00000653893.1:n.2623A>C
ENST00000654170.1:n.2608A>C
ENST00000656114.1:n.2851A>C
ENST00000656590.1:c.6692A>C
ENST00000658083.1:n.2945A>C
ENST00000661310.1:c.7573A>C ENSP00000499589.1:p.Lys2525Gln
ENST00000665483.1:n.5305A>C
ENST00000666447.1:n.4268A>C
ENST00000666943.1:n.4497A>C
ENST00000350721.8:c.7765A>C ENSP00000343741.4:p.Lys2589Gln
ENST00000504521.5:c.354A>C ENSP00000422553.1:n.354A>C
ENST00000513291.1:c.4829A>C
ENST00000515810.1:c.191A>C ENSP00000421870.1:n.191A>C
NM_001184.3:c.7765A>C NP_001175.2:p.Lys2589Gln
XM_011512924.1:c.7771A>C XP_011511226.1:p.Lys2591Gln
XM_011512925.1:c.7579A>C XP_011511227.1:p.Lys2527Gln
XR_924147.1:n.10522A>C
XR_924148.1:n.7997A>C
NM_001354579.1:c.7573A>C NP_001341508.1:p.Lys2525Gln
XR_001740179.2:n.7991A>C
XR_924148.2:n.7997A>C
NM_001184.4:c.7765A>C MANE Select NP_001175.2:p.Lys2589Gln
NM_001354579.2:c.7573A>C NP_001341508.1:p.Lys2525Gln