Canonical Allele Identifier: CA1406991909

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470222G= , CM000665.2:g.142470222G=	GRCh38
NC_000003.11:g.142189064G= , CM000665.1:g.142189064G=	GRCh37
NC_000003.10:g.143671754G=	NCBI36
NG_008951.1:g.113605C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-39C= MANE Select	ENSP00000343741.4:n.6222-39C=
ENST00000513291.2:n.1406-39C=
ENST00000654170.1:n.1065-39C=
ENST00000656590.1:c.5012-39C=
ENST00000661310.1:c.6030-39C=	ENSP00000499589.1:n.6030-39C=
ENST00000665483.1:n.77-39C=
ENST00000666447.1:n.57-39C=
ENST00000666943.1:n.1686-39C=
ENST00000350721.8:c.6222-39C=	ENSP00000343741.4:n.6222-39C=
NM_001184.3:c.6222-39C=	NP_001175.2:n.6222-39C=
XM_011512924.1:c.6228-39C=	XP_011511226.1:n.6228-39C=
XM_011512925.1:c.6036-39C=	XP_011511227.1:n.6036-39C=
XR_924147.1:n.6317-39C=
XR_924148.1:n.6317-39C=
XR_924149.1:n.6196-39C=
NM_001354579.1:c.6030-39C=	NP_001341508.1:n.6030-39C=
XR_001740179.2:n.6311-39C=
XR_001740180.2:n.6365-39C=
XR_001740181.2:n.6244-39C=
XR_001740182.1:n.6196-39C=
XR_002959543.1:n.6421-39C=
XR_924148.2:n.6317-39C=
NM_001184.4:c.6222-39C= MANE Select	NP_001175.2:n.6222-39C=
NM_001354579.2:c.6030-39C=	NP_001341508.1:n.6030-39C=