Canonical Allele Identifier: CA354805501
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470089T>G , CM000665.2:g.142470089T>G GRCh38
NC_000003.11:g.142188931T>G , CM000665.1:g.142188931T>G GRCh37
NC_000003.10:g.143671621T>G NCBI36
NG_008951.1:g.113738A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6316A>C MANE Select ENSP00000343741.4:p.Lys2106Gln
ENST00000513291.2:n.1500A>C
ENST00000654170.1:n.1159A>C
ENST00000656590.1:c.5106A>C
ENST00000661310.1:c.6124A>C ENSP00000499589.1:p.Lys2042Gln
ENST00000665483.1:n.171A>C
ENST00000666447.1:n.151A>C
ENST00000666943.1:n.1780A>C
ENST00000350721.8:c.6316A>C ENSP00000343741.4:p.Lys2106Gln
NM_001184.3:c.6316A>C NP_001175.2:p.Lys2106Gln
XM_011512924.1:c.6322A>C XP_011511226.1:p.Lys2108Gln
XM_011512925.1:c.6130A>C XP_011511227.1:p.Lys2044Gln
XR_924147.1:n.6411A>C
XR_924148.1:n.6411A>C
XR_924149.1:n.6290A>C
NM_001354579.1:c.6124A>C NP_001341508.1:p.Lys2042Gln
XR_001740179.2:n.6405A>C
XR_001740180.2:n.6459A>C
XR_001740181.2:n.6338A>C
XR_001740182.1:n.6290A>C
XR_002959543.1:n.6515A>C
XR_924148.2:n.6411A>C
NM_001184.4:c.6316A>C MANE Select NP_001175.2:p.Lys2106Gln
NM_001354579.2:c.6124A>C NP_001341508.1:p.Lys2042Gln