Canonical Allele Identifier: CA1406990140

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142465860G= , CM000665.2:g.142465860G=	GRCh38
NC_000003.11:g.142184702G= , CM000665.1:g.142184702G=	GRCh37
NC_000003.10:g.143667392G=	NCBI36
NG_008951.1:g.117967C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6897+464C= MANE Select	ENSP00000343741.4:n.6897+464C=
ENST00000513291.2:n.2081+464C=
ENST00000654170.1:n.1740+464C=
ENST00000656590.1:c.5687+464C=
ENST00000661310.1:c.6705+464C=	ENSP00000499589.1:n.6705+464C=
ENST00000665483.1:n.2616C=
ENST00000666447.1:n.3400+464C=
ENST00000666943.1:n.3629+464C=
ENST00000350721.8:c.6897+464C=	ENSP00000343741.4:n.6897+464C=
ENST00000513291.1:c.436+464C=
NM_001184.3:c.6897+464C=	NP_001175.2:n.6897+464C=
XM_011512924.1:c.6903+464C=	XP_011511226.1:n.6903+464C=
XM_011512925.1:c.6711+464C=	XP_011511227.1:n.6711+464C=
XR_924147.1:n.6992+464C=
XR_924148.1:n.6992+464C=
NM_001354579.1:c.6705+464C=	NP_001341508.1:n.6705+464C=
XR_001740179.2:n.6986+464C=
XR_924148.2:n.6992+464C=
NM_001184.4:c.6897+464C= MANE Select	NP_001175.2:n.6897+464C=
NM_001354579.2:c.6705+464C=	NP_001341508.1:n.6705+464C=