Canonical Allele Identifier: CA354805815
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470142G>C , CM000665.2:g.142470142G>C GRCh38
NC_000003.11:g.142188984G>C , CM000665.1:g.142188984G>C GRCh37
NC_000003.10:g.143671674G>C NCBI36
NG_008951.1:g.113685C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6263C>G MANE Select ENSP00000343741.4:p.Pro2088Arg
ENST00000513291.2:n.1447C>G
ENST00000654170.1:n.1106C>G
ENST00000656590.1:c.5053C>G
ENST00000661310.1:c.6071C>G ENSP00000499589.1:p.Pro2024Arg
ENST00000665483.1:n.118C>G
ENST00000666447.1:n.98C>G
ENST00000666943.1:n.1727C>G
ENST00000350721.8:c.6263C>G ENSP00000343741.4:p.Pro2088Arg
NM_001184.3:c.6263C>G NP_001175.2:p.Pro2088Arg
XM_011512924.1:c.6269C>G XP_011511226.1:p.Pro2090Arg
XM_011512925.1:c.6077C>G XP_011511227.1:p.Pro2026Arg
XR_924147.1:n.6358C>G
XR_924148.1:n.6358C>G
XR_924149.1:n.6237C>G
NM_001354579.1:c.6071C>G NP_001341508.1:p.Pro2024Arg
XR_001740179.2:n.6352C>G
XR_001740180.2:n.6406C>G
XR_001740181.2:n.6285C>G
XR_001740182.1:n.6237C>G
XR_002959543.1:n.6462C>G
XR_924148.2:n.6358C>G
NM_001184.4:c.6263C>G MANE Select NP_001175.2:p.Pro2088Arg
NM_001354579.2:c.6071C>G NP_001341508.1:p.Pro2024Arg