Canonical Allele Identifier: CA436120059

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142453224C>T , CM000665.2:g.142453224C>T	GRCh38
NC_000003.11:g.142172066C>T , CM000665.1:g.142172066C>T	GRCh37
NC_000003.10:g.143654756C>T	NCBI36
NG_008951.1:g.130603G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001184.4:c.7665G>A MANE Select	NP_001175.2:p.Lys2555=
ENST00000350721.9:c.7665G>A MANE Select	ENSP00000343741.4:p.Lys2555=
NM_001184.3:c.7665G>A	NP_001175.2:p.Lys2555=
NM_001354579.1:c.7473G>A	NP_001341508.1:p.Lys2491=
NM_001354579.2:c.7473G>A	NP_001341508.1:p.Lys2491=
ENST00000350721.8:c.7665G>A	ENSP00000343741.4:p.Lys2555=
ENST00000504521.5:c.117G>A	ENSP00000422553.1:p.Lys39=
ENST00000511016.1:n.210G>A
ENST00000513291.1:c.1204G>A
ENST00000513291.2:n.2849G>A
ENST00000653893.1:n.2523G>A
ENST00000654170.1:n.2508G>A
ENST00000656114.1:n.2751G>A
ENST00000656590.1:c.6455G>A
ENST00000658083.1:n.2708G>A
ENST00000661310.1:c.7473G>A	ENSP00000499589.1:p.Lys2491=
ENST00000665483.1:n.5205G>A
ENST00000666447.1:n.4168G>A
ENST00000666943.1:n.4397G>A
XM_011512924.1:c.7671G>A	XP_011511226.1:p.Lys2557=
XM_011512925.1:c.7479G>A	XP_011511227.1:p.Lys2493=
XR_001740179.2:n.7754G>A
XR_924147.1:n.7760G>A
XR_924148.1:n.7760G>A
XR_924148.2:n.7760G>A