Canonical Allele Identifier: CA354805762
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470133A>C , CM000665.2:g.142470133A>C GRCh38
NC_000003.11:g.142188975A>C , CM000665.1:g.142188975A>C GRCh37
NC_000003.10:g.143671665A>C NCBI36
NG_008951.1:g.113694T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6272T>G MANE Select ENSP00000343741.4:p.Leu2091Ter
ENST00000513291.2:n.1456T>G
ENST00000654170.1:n.1115T>G
ENST00000656590.1:c.5062T>G
ENST00000661310.1:c.6080T>G ENSP00000499589.1:p.Leu2027Ter
ENST00000665483.1:n.127T>G
ENST00000666447.1:n.107T>G
ENST00000666943.1:n.1736T>G
ENST00000350721.8:c.6272T>G ENSP00000343741.4:p.Leu2091Ter
NM_001184.3:c.6272T>G NP_001175.2:p.Leu2091Ter
XM_011512924.1:c.6278T>G XP_011511226.1:p.Leu2093Ter
XM_011512925.1:c.6086T>G XP_011511227.1:p.Leu2029Ter
XR_924147.1:n.6367T>G
XR_924148.1:n.6367T>G
XR_924149.1:n.6246T>G
NM_001354579.1:c.6080T>G NP_001341508.1:p.Leu2027Ter
XR_001740179.2:n.6361T>G
XR_001740180.2:n.6415T>G
XR_001740181.2:n.6294T>G
XR_001740182.1:n.6246T>G
XR_002959543.1:n.6471T>G
XR_924148.2:n.6367T>G
NM_001184.4:c.6272T>G MANE Select NP_001175.2:p.Leu2091Ter
NM_001354579.2:c.6080T>G NP_001341508.1:p.Leu2027Ter