Canonical Allele Identifier: CA1406991870
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470104C= , CM000665.2:g.142470104C= GRCh38
NC_000003.11:g.142188946C= , CM000665.1:g.142188946C= GRCh37
NC_000003.10:g.143671636C= NCBI36
NG_008951.1:g.113723G=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6301G= MANE Select ENSP00000343741.4:p.Ala2101=
ENST00000513291.2:n.1485G=
ENST00000654170.1:n.1144G=
ENST00000656590.1:c.5091G=
ENST00000661310.1:c.6109G= ENSP00000499589.1:p.Ala2037=
ENST00000665483.1:n.156G=
ENST00000666447.1:n.136G=
ENST00000666943.1:n.1765G=
ENST00000350721.8:c.6301G= ENSP00000343741.4:p.Ala2101=
NM_001184.3:c.6301G= NP_001175.2:p.Ala2101=
XM_011512924.1:c.6307G= XP_011511226.1:p.Ala2103=
XM_011512925.1:c.6115G= XP_011511227.1:p.Ala2039=
XR_924147.1:n.6396G=
XR_924148.1:n.6396G=
XR_924149.1:n.6275G=
NM_001354579.1:c.6109G= NP_001341508.1:p.Ala2037=
XR_001740179.2:n.6390G=
XR_001740180.2:n.6444G=
XR_001740181.2:n.6323G=
XR_001740182.1:n.6275G=
XR_002959543.1:n.6500G=
XR_924148.2:n.6396G=
NM_001184.4:c.6301G= MANE Select NP_001175.2:p.Ala2101=
NM_001354579.2:c.6109G= NP_001341508.1:p.Ala2037=