Canonical Allele Identifier: CA1406991989

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470405C= , CM000665.2:g.142470405C=	GRCh38
NC_000003.11:g.142189247C= , CM000665.1:g.142189247C=	GRCh37
NC_000003.10:g.143671937C=	NCBI36
NG_008951.1:g.113422G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-222G= MANE Select	ENSP00000343741.4:n.6222-222G=
ENST00000513291.2:n.1406-222G=
ENST00000654170.1:n.1065-222G=
ENST00000656590.1:c.5012-222G=
ENST00000661310.1:c.6030-222G=	ENSP00000499589.1:n.6030-222G=
ENST00000665483.1:n.77-222G=
ENST00000666447.1:n.57-222G=
ENST00000666943.1:n.1686-222G=
ENST00000350721.8:c.6222-222G=	ENSP00000343741.4:n.6222-222G=
NM_001184.3:c.6222-222G=	NP_001175.2:n.6222-222G=
XM_011512924.1:c.6228-222G=	XP_011511226.1:n.6228-222G=
XM_011512925.1:c.6036-222G=	XP_011511227.1:n.6036-222G=
XR_924147.1:n.6317-222G=
XR_924148.1:n.6317-222G=
XR_924149.1:n.6196-222G=
NM_001354579.1:c.6030-222G=	NP_001341508.1:n.6030-222G=
XR_001740179.2:n.6311-222G=
XR_001740180.2:n.6365-222G=
XR_001740181.2:n.6244-222G=
XR_001740182.1:n.6196-222G=
XR_002959543.1:n.6421-222G=
XR_924148.2:n.6317-222G=
NM_001184.4:c.6222-222G= MANE Select	NP_001175.2:n.6222-222G=
NM_001354579.2:c.6030-222G=	NP_001341508.1:n.6030-222G=