Canonical Allele Identifier: CA354796816
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142513537A>C , CM000665.2:g.142513537A>C GRCh38
NC_000003.11:g.142232379A>C , CM000665.1:g.142232379A>C GRCh37
NC_000003.10:g.143715069A>C NCBI36
NG_008951.1:g.70290T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.4605T>G MANE Select ENSP00000343741.4:p.Tyr1535Ter
ENST00000653868.1:n.4634T>G
ENST00000656590.1:c.3395T>G
ENST00000661310.1:c.4413T>G ENSP00000499589.1:p.Tyr1471Ter
ENST00000666943.1:n.69T>G
ENST00000350721.8:c.4605T>G ENSP00000343741.4:p.Tyr1535Ter
NM_001184.3:c.4605T>G NP_001175.2:p.Tyr1535Ter
XM_011512924.1:c.4611T>G XP_011511226.1:p.Tyr1537Ter
XM_011512925.1:c.4419T>G XP_011511227.1:p.Tyr1473Ter
XM_011512926.1:c.4611T>G XP_011511228.1:p.Tyr1537Ter
XM_011512927.1:c.4611T>G XP_011511229.1:p.Tyr1537Ter
XR_924147.1:n.4700T>G
XR_924148.1:n.4700T>G
XR_924149.1:n.4700T>G
NM_001354579.1:c.4413T>G NP_001341508.1:p.Tyr1471Ter
XR_001740179.2:n.4694T>G
XR_001740180.2:n.4700T>G
XR_001740181.2:n.4700T>G
XR_001740182.1:n.4700T>G
XR_002959543.1:n.4700T>G
XR_924148.2:n.4700T>G
NM_001184.4:c.4605T>G MANE Select NP_001175.2:p.Tyr1535Ter
NM_001354579.2:c.4413T>G NP_001341508.1:p.Tyr1471Ter