Canonical Allele Identifier: CA1406978081

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142449648G= , CM000665.2:g.142449648G=	GRCh38
NC_000003.11:g.142168490G= , CM000665.1:g.142168490G=	GRCh37
NC_000003.10:g.143651180G=	NCBI36
NG_008951.1:g.134179C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.7762-46C= MANE Select	ENSP00000343741.4:n.7762-46C=
ENST00000513291.2:n.6425C=
ENST00000653893.1:n.2620-46C=
ENST00000654170.1:n.2605-46C=
ENST00000656114.1:n.2848-46C=
ENST00000656590.1:c.6689-46C=
ENST00000658083.1:n.2942-46C=
ENST00000661310.1:c.7570-46C=	ENSP00000499589.1:n.7570-46C=
ENST00000665483.1:n.5302-46C=
ENST00000666447.1:n.4265-46C=
ENST00000666943.1:n.4494-46C=
ENST00000350721.8:c.7762-46C=	ENSP00000343741.4:n.7762-46C=
ENST00000504521.5:c.351-46C=	ENSP00000422553.1:n.351-46C=
ENST00000513291.1:c.4780C=
ENST00000515810.1:c.188-46C=	ENSP00000421870.1:n.188-46C=
NM_001184.3:c.7762-46C=	NP_001175.2:n.7762-46C=
XM_011512924.1:c.7768-46C=	XP_011511226.1:n.7768-46C=
XM_011512925.1:c.7576-46C=	XP_011511227.1:n.7576-46C=
XR_924147.1:n.10519-46C=
XR_924148.1:n.7994-46C=
NM_001354579.1:c.7570-46C=	NP_001341508.1:n.7570-46C=
XR_001740179.2:n.7988-46C=
XR_924148.2:n.7994-46C=
NM_001184.4:c.7762-46C= MANE Select	NP_001175.2:n.7762-46C=
NM_001354579.2:c.7570-46C=	NP_001341508.1:n.7570-46C=