Canonical Allele Identifier: CA1407006747
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142498152A= , CM000665.2:g.142498152A= GRCh38
NC_000003.11:g.142216994A= , CM000665.1:g.142216994A= GRCh37
NC_000003.10:g.143699684A= NCBI36
NG_008951.1:g.85675T=

Transcript Alleles

HGVS Amino-acid change
ENST00000350721.9:c.5558+445T= MANE Select ENSP00000343741.4:n.5558+445T=
ENST00000513291.2:n.742+445T=
ENST00000653868.1:n.5587+445T=
ENST00000656590.1:c.4348+445T=
ENST00000661310.1:c.5366+445T= ENSP00000499589.1:n.5366+445T=
ENST00000666943.1:n.1022+445T=
ENST00000350721.8:c.5558+445T= ENSP00000343741.4:n.5558+445T=
ENST00000507620.2:n.654+445T=
ENST00000514393.5:n.241+445T=
NM_001184.3:c.5558+445T= NP_001175.2:n.5558+445T=
XM_011512924.1:c.5564+445T= XP_011511226.1:n.5564+445T=
XM_011512925.1:c.5372+445T= XP_011511227.1:n.5372+445T=
XM_011512926.1:c.5564+445T= XP_011511228.1:n.5564+445T=
XM_011512927.1:c.5564+445T= XP_011511229.1:n.5564+445T=
XR_924147.1:n.5653+445T=
XR_924148.1:n.5653+445T=
XR_924149.1:n.5653+445T=
NM_001354579.1:c.5366+445T= NP_001341508.1:n.5366+445T=
XR_001740179.2:n.5647+445T=
XR_001740180.2:n.5653+445T=
XR_001740181.2:n.5653+445T=
XR_001740182.1:n.5653+445T=
XR_002959543.1:n.5653+445T=
XR_924148.2:n.5653+445T=
NM_001184.4:c.5558+445T= MANE Select NP_001175.2:n.5558+445T=
NM_001354579.2:c.5366+445T= NP_001341508.1:n.5366+445T=