Canonical Allele Identifier: CA1406991585

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142469363T= , CM000665.2:g.142469363T=	GRCh38
NC_000003.11:g.142188205T= , CM000665.1:g.142188205T=	GRCh37
NC_000003.10:g.143670895T=	NCBI36
NG_008951.1:g.114464A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6526A= MANE Select	ENSP00000343741.4:p.Met2176=
ENST00000513291.2:n.1710A=
ENST00000654170.1:n.1369A=
ENST00000656590.1:c.5316A=
ENST00000661310.1:c.6334A=	ENSP00000499589.1:p.Met2112=
ENST00000665483.1:n.381A=
ENST00000666447.1:n.361A=
ENST00000666943.1:n.1990A=
ENST00000350721.8:c.6526A=	ENSP00000343741.4:p.Met2176=
ENST00000513291.1:c.65A=
NM_001184.3:c.6526A=	NP_001175.2:p.Met2176=
XM_011512924.1:c.6532A=	XP_011511226.1:p.Met2178=
XM_011512925.1:c.6340A=	XP_011511227.1:p.Met2114=
XR_924147.1:n.6621A=
XR_924148.1:n.6621A=
XR_924149.1:n.6500A=
NM_001354579.1:c.6334A=	NP_001341508.1:p.Met2112=
XR_001740179.2:n.6615A=
XR_924148.2:n.6621A=
NM_001184.4:c.6526A= MANE Select	NP_001175.2:p.Met2176=
NM_001354579.2:c.6334A=	NP_001341508.1:p.Met2112=