Canonical Allele Identifier: CA1406991884
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470159G= , CM000665.2:g.142470159G= GRCh38
NC_000003.11:g.142189001G= , CM000665.1:g.142189001G= GRCh37
NC_000003.10:g.143671691G= NCBI36
NG_008951.1:g.113668C=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6246C= MANE Select ENSP00000343741.4:p.Phe2082=
ENST00000513291.2:n.1430C=
ENST00000654170.1:n.1089C=
ENST00000656590.1:c.5036C=
ENST00000661310.1:c.6054C= ENSP00000499589.1:p.Phe2018=
ENST00000665483.1:n.101C=
ENST00000666447.1:n.81C=
ENST00000666943.1:n.1710C=
ENST00000350721.8:c.6246C= ENSP00000343741.4:p.Phe2082=
NM_001184.3:c.6246C= NP_001175.2:p.Phe2082=
XM_011512924.1:c.6252C= XP_011511226.1:p.Phe2084=
XM_011512925.1:c.6060C= XP_011511227.1:p.Phe2020=
XR_924147.1:n.6341C=
XR_924148.1:n.6341C=
XR_924149.1:n.6220C=
NM_001354579.1:c.6054C= NP_001341508.1:p.Phe2018=
XR_001740179.2:n.6335C=
XR_001740180.2:n.6389C=
XR_001740181.2:n.6268C=
XR_001740182.1:n.6220C=
XR_002959543.1:n.6445C=
XR_924148.2:n.6341C=
NM_001184.4:c.6246C= MANE Select NP_001175.2:p.Phe2082=
NM_001354579.2:c.6054C= NP_001341508.1:p.Phe2018=