Canonical Allele Identifier: CA354805493
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470088T>C , CM000665.2:g.142470088T>C GRCh38
NC_000003.11:g.142188930T>C , CM000665.1:g.142188930T>C GRCh37
NC_000003.10:g.143671620T>C NCBI36
NG_008951.1:g.113739A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6317A>G MANE Select ENSP00000343741.4:p.Lys2106Arg
ENST00000513291.2:n.1501A>G
ENST00000654170.1:n.1160A>G
ENST00000656590.1:c.5107A>G
ENST00000661310.1:c.6125A>G ENSP00000499589.1:p.Lys2042Arg
ENST00000665483.1:n.172A>G
ENST00000666447.1:n.152A>G
ENST00000666943.1:n.1781A>G
ENST00000350721.8:c.6317A>G ENSP00000343741.4:p.Lys2106Arg
NM_001184.3:c.6317A>G NP_001175.2:p.Lys2106Arg
XM_011512924.1:c.6323A>G XP_011511226.1:p.Lys2108Arg
XM_011512925.1:c.6131A>G XP_011511227.1:p.Lys2044Arg
XR_924147.1:n.6412A>G
XR_924148.1:n.6412A>G
XR_924149.1:n.6291A>G
NM_001354579.1:c.6125A>G NP_001341508.1:p.Lys2042Arg
XR_001740179.2:n.6406A>G
XR_001740180.2:n.6460A>G
XR_001740181.2:n.6339A>G
XR_001740182.1:n.6291A>G
XR_002959543.1:n.6516A>G
XR_924148.2:n.6412A>G
NM_001184.4:c.6317A>G MANE Select NP_001175.2:p.Lys2106Arg
NM_001354579.2:c.6125A>G NP_001341508.1:p.Lys2042Arg