Canonical Allele Identifier: CA1406991769

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469827A= , CM000665.2:g.142469827A=	GRCh38
NC_000003.11:g.142188669A= , CM000665.1:g.142188669A=	GRCh37
NC_000003.10:g.143671359A=	NCBI36
NG_008951.1:g.114000T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6320-258T= MANE Select	ENSP00000343741.4:n.6320-258T=
ENST00000513291.2:n.1504-258T=
ENST00000654170.1:n.1163-258T=
ENST00000656590.1:c.5110-258T=
ENST00000661310.1:c.6128-258T=	ENSP00000499589.1:n.6128-258T=
ENST00000665483.1:n.175-258T=
ENST00000666447.1:n.155-258T=
ENST00000666943.1:n.1784-258T=
ENST00000350721.8:c.6320-258T=	ENSP00000343741.4:n.6320-258T=
NM_001184.3:c.6320-258T=	NP_001175.2:n.6320-258T=
XM_011512924.1:c.6326-258T=	XP_011511226.1:n.6326-258T=
XM_011512925.1:c.6134-258T=	XP_011511227.1:n.6134-258T=
XR_924147.1:n.6415-258T=
XR_924148.1:n.6415-258T=
XR_924149.1:n.6294-258T=
NM_001354579.1:c.6128-258T=	NP_001341508.1:n.6128-258T=
XR_001740179.2:n.6409-258T=
XR_001740180.2:n.6463-258T=
XR_001740181.2:n.6342-258T=
XR_001740182.1:n.6294-258T=
XR_002959543.1:n.6519-258T=
XR_924148.2:n.6415-258T=
NM_001184.4:c.6320-258T= MANE Select	NP_001175.2:n.6320-258T=
NM_001354579.2:c.6128-258T=	NP_001341508.1:n.6128-258T=