Canonical Allele Identifier: CA1406991878
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470136A= , CM000665.2:g.142470136A= GRCh38
NC_000003.11:g.142188978A= , CM000665.1:g.142188978A= GRCh37
NC_000003.10:g.143671668A= NCBI36
NG_008951.1:g.113691T=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6269T= MANE Select ENSP00000343741.4:p.Met2090=
ENST00000513291.2:n.1453T=
ENST00000654170.1:n.1112T=
ENST00000656590.1:c.5059T=
ENST00000661310.1:c.6077T= ENSP00000499589.1:p.Met2026=
ENST00000665483.1:n.124T=
ENST00000666447.1:n.104T=
ENST00000666943.1:n.1733T=
ENST00000350721.8:c.6269T= ENSP00000343741.4:p.Met2090=
NM_001184.3:c.6269T= NP_001175.2:p.Met2090=
XM_011512924.1:c.6275T= XP_011511226.1:p.Met2092=
XM_011512925.1:c.6083T= XP_011511227.1:p.Met2028=
XR_924147.1:n.6364T=
XR_924148.1:n.6364T=
XR_924149.1:n.6243T=
NM_001354579.1:c.6077T= NP_001341508.1:p.Met2026=
XR_001740179.2:n.6358T=
XR_001740180.2:n.6412T=
XR_001740181.2:n.6291T=
XR_001740182.1:n.6243T=
XR_002959543.1:n.6468T=
XR_924148.2:n.6364T=
NM_001184.4:c.6269T= MANE Select NP_001175.2:p.Met2090=
NM_001354579.2:c.6077T= NP_001341508.1:p.Met2026=