Canonical Allele Identifier: CA354825962
Gene: ATR HGNC NCBI

Linked Data

ClinVar Variation Id: 1756468
ClinVar RCV Id: RCV002364676
dbSNP Id: rs2108487899

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142562704C>T , CM000665.2:g.142562704C>T GRCh38
NC_000003.11:g.142281546C>T , CM000665.1:g.142281546C>T GRCh37
NC_000003.10:g.143764236C>T NCBI36
NG_008951.1:g.21123G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.698G>A MANE Select ENSP00000343741.4:p.Gly233Asp
ENST00000515149.3:c.293-1283G>A ENSP00000425897.3:n.293-1283G>A
ENST00000653868.1:n.727G>A
ENST00000657914.1:n.3056G>A
ENST00000659195.1:n.2763G>A
ENST00000661310.1:c.698G>A ENSP00000499589.1:p.Gly233Asp
ENST00000350721.8:c.698G>A ENSP00000343741.4:p.Gly233Asp
ENST00000507148.1:c.293-356G>A ENSP00000426595.1:n.293-356G>A
NM_001184.3:c.698G>A NP_001175.2:p.Gly233Asp
XM_011512924.1:c.698G>A XP_011511226.1:p.Gly233Asp
XM_011512925.1:c.698G>A XP_011511227.1:p.Gly233Asp
XM_011512926.1:c.698G>A XP_011511228.1:p.Gly233Asp
XM_011512927.1:c.698G>A XP_011511229.1:p.Gly233Asp
XR_924147.1:n.787G>A
XR_924148.1:n.787G>A
XR_924149.1:n.787G>A
NM_001354579.1:c.698G>A NP_001341508.1:p.Gly233Asp
XR_001740179.2:n.787G>A
XR_001740180.2:n.787G>A
XR_001740181.2:n.787G>A
XR_001740182.1:n.787G>A
XR_002959543.1:n.787G>A
XR_924148.2:n.787G>A
NM_001184.4:c.698G>A MANE Select NP_001175.2:p.Gly233Asp
NM_001354579.2:c.698G>A NP_001341508.1:p.Gly233Asp