Canonical Allele Identifier: CA84759780

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142496275C>T , CM000665.2:g.142496275C>T	GRCh38
NC_000003.11:g.142215117C>T , CM000665.1:g.142215117C>T	GRCh37
NC_000003.10:g.143697807C>T	NCBI36
NG_008951.1:g.87552G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.5898+86G>A MANE Select	ENSP00000343741.4:n.5898+86G>A
ENST00000513291.2:n.1082+86G>A
ENST00000653868.1:n.5927+86G>A
ENST00000656590.1:c.4688+86G>A
ENST00000661310.1:c.5706+86G>A	ENSP00000499589.1:n.5706+86G>A
ENST00000666943.1:n.1362+86G>A
ENST00000350721.8:c.5898+86G>A	ENSP00000343741.4:n.5898+86G>A
NM_001184.3:c.5898+86G>A	NP_001175.2:n.5898+86G>A
XM_011512924.1:c.5904+86G>A	XP_011511226.1:n.5904+86G>A
XM_011512925.1:c.5712+86G>A	XP_011511227.1:n.5712+86G>A
XM_011512926.1:c.5904+86G>A	XP_011511228.1:n.5904+86G>A
XM_011512927.1:c.5904+86G>A	XP_011511229.1:n.5904+86G>A
XR_924147.1:n.5993+86G>A
XR_924148.1:n.5993+86G>A
XR_924149.1:n.5872+86G>A
NM_001354579.1:c.5706+86G>A	NP_001341508.1:n.5706+86G>A
XR_001740179.2:n.5987+86G>A
XR_001740180.2:n.5993+86G>A
XR_001740181.2:n.5872+86G>A
XR_001740182.1:n.5872+86G>A
XR_002959543.1:n.5993+86G>A
XR_924148.2:n.5993+86G>A
NM_001184.4:c.5898+86G>A MANE Select	NP_001175.2:n.5898+86G>A
NM_001354579.2:c.5706+86G>A	NP_001341508.1:n.5706+86G>A