Canonical Allele Identifier: CA354805694
Gene: ATR HGNC NCBI

Linked Data

dbSNP Id: rs2108280745
COSMIC: COSM419785

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470128G>C , CM000665.2:g.142470128G>C GRCh38
NC_000003.11:g.142188970G>C , CM000665.1:g.142188970G>C GRCh37
NC_000003.10:g.143671660G>C NCBI36
NG_008951.1:g.113699C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6277C>G MANE Select ENSP00000343741.4:p.Leu2093Val
ENST00000513291.2:n.1461C>G
ENST00000654170.1:n.1120C>G
ENST00000656590.1:c.5067C>G
ENST00000661310.1:c.6085C>G ENSP00000499589.1:p.Leu2029Val
ENST00000665483.1:n.132C>G
ENST00000666447.1:n.112C>G
ENST00000666943.1:n.1741C>G
ENST00000350721.8:c.6277C>G ENSP00000343741.4:p.Leu2093Val
NM_001184.3:c.6277C>G NP_001175.2:p.Leu2093Val
XM_011512924.1:c.6283C>G XP_011511226.1:p.Leu2095Val
XM_011512925.1:c.6091C>G XP_011511227.1:p.Leu2031Val
XR_924147.1:n.6372C>G
XR_924148.1:n.6372C>G
XR_924149.1:n.6251C>G
NM_001354579.1:c.6085C>G NP_001341508.1:p.Leu2029Val
XR_001740179.2:n.6366C>G
XR_001740180.2:n.6420C>G
XR_001740181.2:n.6299C>G
XR_001740182.1:n.6251C>G
XR_002959543.1:n.6476C>G
XR_924148.2:n.6372C>G
NM_001184.4:c.6277C>G MANE Select NP_001175.2:p.Leu2093Val
NM_001354579.2:c.6085C>G NP_001341508.1:p.Leu2029Val