Canonical Allele Identifier: CA354797122
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513616T>A , CM000665.2:g.142513616T>A GRCh38
NC_000003.11:g.142232458T>A , CM000665.1:g.142232458T>A GRCh37
NC_000003.10:g.143715148T>A NCBI36
NG_008951.1:g.70211A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.4526A>T MANE Select ENSP00000343741.4:p.Lys1509Ile
ENST00000653868.1:n.4555A>T
ENST00000656590.1:c.3316A>T
ENST00000661310.1:c.4334A>T ENSP00000499589.1:p.Lys1445Ile
ENST00000350721.8:c.4526A>T ENSP00000343741.4:p.Lys1509Ile
NM_001184.3:c.4526A>T NP_001175.2:p.Lys1509Ile
XM_011512924.1:c.4532A>T XP_011511226.1:p.Lys1511Ile
XM_011512925.1:c.4340A>T XP_011511227.1:p.Lys1447Ile
XM_011512926.1:c.4532A>T XP_011511228.1:p.Lys1511Ile
XM_011512927.1:c.4532A>T XP_011511229.1:p.Lys1511Ile
XR_924147.1:n.4621A>T
XR_924148.1:n.4621A>T
XR_924149.1:n.4621A>T
NM_001354579.1:c.4334A>T NP_001341508.1:p.Lys1445Ile
XR_001740179.2:n.4615A>T
XR_001740180.2:n.4621A>T
XR_001740181.2:n.4621A>T
XR_001740182.1:n.4621A>T
XR_002959543.1:n.4621A>T
XR_924148.2:n.4621A>T
NM_001184.4:c.4526A>T MANE Select NP_001175.2:p.Lys1509Ile
NM_001354579.2:c.4334A>T NP_001341508.1:p.Lys1445Ile