Canonical Allele Identifier: CA1406991809

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469917A= , CM000665.2:g.142469917A=	GRCh38
NC_000003.11:g.142188759A= , CM000665.1:g.142188759A=	GRCh37
NC_000003.10:g.143671449A=	NCBI36
NG_008951.1:g.113910T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6319+169T= MANE Select	ENSP00000343741.4:n.6319+169T=
ENST00000513291.2:n.1503+169T=
ENST00000654170.1:n.1162+169T=
ENST00000656590.1:c.5109+169T=
ENST00000661310.1:c.6127+169T=	ENSP00000499589.1:n.6127+169T=
ENST00000665483.1:n.174+169T=
ENST00000666447.1:n.154+169T=
ENST00000666943.1:n.1783+169T=
ENST00000350721.8:c.6319+169T=	ENSP00000343741.4:n.6319+169T=
NM_001184.3:c.6319+169T=	NP_001175.2:n.6319+169T=
XM_011512924.1:c.6325+169T=	XP_011511226.1:n.6325+169T=
XM_011512925.1:c.6133+169T=	XP_011511227.1:n.6133+169T=
XR_924147.1:n.6414+169T=
XR_924148.1:n.6414+169T=
XR_924149.1:n.6293+169T=
NM_001354579.1:c.6127+169T=	NP_001341508.1:n.6127+169T=
XR_001740179.2:n.6408+169T=
XR_001740180.2:n.6462+169T=
XR_001740181.2:n.6341+169T=
XR_001740182.1:n.6293+169T=
XR_002959543.1:n.6518+169T=
XR_924148.2:n.6414+169T=
NM_001184.4:c.6319+169T= MANE Select	NP_001175.2:n.6319+169T=
NM_001354579.2:c.6127+169T=	NP_001341508.1:n.6127+169T=