Canonical Allele Identifier: CA1407026165

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142549460T= , CM000665.2:g.142549460T=	GRCh38
NC_000003.11:g.142268302T= , CM000665.1:g.142268302T=	GRCh37
NC_000003.10:g.143750992T=	NCBI36
NG_008951.1:g.34367A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.3171+19A= MANE Select	ENSP00000343741.4:n.3171+19A=
ENST00000515149.3:c.*1945+19A=	ENSP00000425897.3:n.*1945+19A=
ENST00000653868.1:n.3200+19A=
ENST00000656582.1:n.430+19A=
ENST00000656590.1:c.1961+19A=
ENST00000661310.1:c.2979+19A=	ENSP00000499589.1:n.2979+19A=
ENST00000350721.8:c.3171+19A=	ENSP00000343741.4:n.3171+19A=
NM_001184.3:c.3171+19A=	NP_001175.2:n.3171+19A=
XM_011512924.1:c.3171+19A=	XP_011511226.1:n.3171+19A=
XM_011512925.1:c.2979+19A=	XP_011511227.1:n.2979+19A=
XM_011512926.1:c.3171+19A=	XP_011511228.1:n.3171+19A=
XM_011512927.1:c.3171+19A=	XP_011511229.1:n.3171+19A=
XR_924147.1:n.3260+19A=
XR_924148.1:n.3260+19A=
XR_924149.1:n.3260+19A=
NM_001354579.1:c.2979+19A=	NP_001341508.1:n.2979+19A=
XR_001740179.2:n.3260+19A=
XR_001740180.2:n.3260+19A=
XR_001740181.2:n.3260+19A=
XR_001740182.1:n.3260+19A=
XR_002959543.1:n.3260+19A=
XR_924148.2:n.3260+19A=
NM_001184.4:c.3171+19A= MANE Select	NP_001175.2:n.3171+19A=
NM_001354579.2:c.2979+19A=	NP_001341508.1:n.2979+19A=