Canonical Allele Identifier: CA1406991863
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142470077G= , CM000665.2:g.142470077G= GRCh38
NC_000003.11:g.142188919G= , CM000665.1:g.142188919G= GRCh37
NC_000003.10:g.143671609G= NCBI36
NG_008951.1:g.113750C=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.6319+9C= MANE Select ENSP00000343741.4:n.6319+9C=
ENST00000513291.2:n.1503+9C=
ENST00000654170.1:n.1162+9C=
ENST00000656590.1:c.5109+9C=
ENST00000661310.1:c.6127+9C= ENSP00000499589.1:n.6127+9C=
ENST00000665483.1:n.174+9C=
ENST00000666447.1:n.154+9C=
ENST00000666943.1:n.1783+9C=
ENST00000350721.8:c.6319+9C= ENSP00000343741.4:n.6319+9C=
NM_001184.3:c.6319+9C= NP_001175.2:n.6319+9C=
XM_011512924.1:c.6325+9C= XP_011511226.1:n.6325+9C=
XM_011512925.1:c.6133+9C= XP_011511227.1:n.6133+9C=
XR_924147.1:n.6414+9C=
XR_924148.1:n.6414+9C=
XR_924149.1:n.6293+9C=
NM_001354579.1:c.6127+9C= NP_001341508.1:n.6127+9C=
XR_001740179.2:n.6408+9C=
XR_001740180.2:n.6462+9C=
XR_001740181.2:n.6341+9C=
XR_001740182.1:n.6293+9C=
XR_002959543.1:n.6518+9C=
XR_924148.2:n.6414+9C=
NM_001184.4:c.6319+9C= MANE Select NP_001175.2:n.6319+9C=
NM_001354579.2:c.6127+9C= NP_001341508.1:n.6127+9C=