Canonical Allele Identifier: CA1407031568

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562338T= , CM000665.2:g.142562338T=	GRCh38
NC_000003.11:g.142281180T= , CM000665.1:g.142281180T=	GRCh37
NC_000003.10:g.143763870T=	NCBI36
NG_008951.1:g.21489A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.1064A= MANE Select	ENSP00000343741.4:p.Lys355=
ENST00000515149.3:c.293-917A=	ENSP00000425897.3:n.293-917A=
ENST00000653868.1:n.1093A=
ENST00000657914.1:n.3422A=
ENST00000659195.1:n.3129A=
ENST00000661310.1:c.1064A=	ENSP00000499589.1:p.Lys355=
ENST00000350721.8:c.1064A=	ENSP00000343741.4:p.Lys355=
ENST00000507148.1:c.303A=	ENSP00000426595.1:p.Ter101=
ENST00000515149.2:c.107A=	ENSP00000425897.2:p.Lys36=
NM_001184.3:c.1064A=	NP_001175.2:p.Lys355=
XM_011512924.1:c.1064A=	XP_011511226.1:p.Lys355=
XM_011512925.1:c.1064A=	XP_011511227.1:p.Lys355=
XM_011512926.1:c.1064A=	XP_011511228.1:p.Lys355=
XM_011512927.1:c.1064A=	XP_011511229.1:p.Lys355=
XR_924147.1:n.1153A=
XR_924148.1:n.1153A=
XR_924149.1:n.1153A=
NM_001354579.1:c.1064A=	NP_001341508.1:p.Lys355=
XR_001740179.2:n.1153A=
XR_001740180.2:n.1153A=
XR_001740181.2:n.1153A=
XR_001740182.1:n.1153A=
XR_002959543.1:n.1153A=
XR_924148.2:n.1153A=
NM_001184.4:c.1064A= MANE Select	NP_001175.2:p.Lys355=
NM_001354579.2:c.1064A=	NP_001341508.1:p.Lys355=