Canonical Allele Identifier: CA1407029582

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553702G= , CM000665.2:g.142553702G=	GRCh38
NC_000003.11:g.142272544G= , CM000665.1:g.142272544G=	GRCh37
NC_000003.10:g.143755234G=	NCBI36
NG_008951.1:g.30125C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2571C= MANE Select	ENSP00000343741.4:p.Ala857=
ENST00000515149.3:c.*1345C=	ENSP00000425897.3:n.*1345C=
ENST00000653868.1:n.2600C=
ENST00000656590.1:c.1361C=
ENST00000659195.1:n.5446C=
ENST00000661310.1:c.2379C=	ENSP00000499589.1:p.Ala793=
ENST00000350721.8:c.2571C=	ENSP00000343741.4:p.Ala857=
NM_001184.3:c.2571C=	NP_001175.2:p.Ala857=
XM_011512924.1:c.2571C=	XP_011511226.1:p.Ala857=
XM_011512925.1:c.2379C=	XP_011511227.1:p.Ala793=
XM_011512926.1:c.2571C=	XP_011511228.1:p.Ala857=
XM_011512927.1:c.2571C=	XP_011511229.1:p.Ala857=
XR_924147.1:n.2660C=
XR_924148.1:n.2660C=
XR_924149.1:n.2660C=
NM_001354579.1:c.2379C=	NP_001341508.1:p.Ala793=
XR_001740179.2:n.2660C=
XR_001740180.2:n.2660C=
XR_001740181.2:n.2660C=
XR_001740182.1:n.2660C=
XR_002959543.1:n.2660C=
XR_924148.2:n.2660C=
NM_001184.4:c.2571C= MANE Select	NP_001175.2:p.Ala857=
NM_001354579.2:c.2379C=	NP_001341508.1:p.Ala793=