Canonical Allele Identifier: CA354806086
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470169C>T , CM000665.2:g.142470169C>T GRCh38
NC_000003.11:g.142189011C>T , CM000665.1:g.142189011C>T GRCh37
NC_000003.10:g.143671701C>T NCBI36
NG_008951.1:g.113658G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.6236G>A MANE Select ENSP00000343741.4:p.Gly2079Glu
ENST00000513291.2:n.1420G>A
ENST00000654170.1:n.1079G>A
ENST00000656590.1:c.5026G>A
ENST00000661310.1:c.6044G>A ENSP00000499589.1:p.Gly2015Glu
ENST00000665483.1:n.91G>A
ENST00000666447.1:n.71G>A
ENST00000666943.1:n.1700G>A
ENST00000350721.8:c.6236G>A ENSP00000343741.4:p.Gly2079Glu
NM_001184.3:c.6236G>A NP_001175.2:p.Gly2079Glu
XM_011512924.1:c.6242G>A XP_011511226.1:p.Gly2081Glu
XM_011512925.1:c.6050G>A XP_011511227.1:p.Gly2017Glu
XR_924147.1:n.6331G>A
XR_924148.1:n.6331G>A
XR_924149.1:n.6210G>A
NM_001354579.1:c.6044G>A NP_001341508.1:p.Gly2015Glu
XR_001740179.2:n.6325G>A
XR_001740180.2:n.6379G>A
XR_001740181.2:n.6258G>A
XR_001740182.1:n.6210G>A
XR_002959543.1:n.6435G>A
XR_924148.2:n.6331G>A
NM_001184.4:c.6236G>A MANE Select NP_001175.2:p.Gly2079Glu
NM_001354579.2:c.6044G>A NP_001341508.1:p.Gly2015Glu