Canonical Allele Identifier: CA2509644609

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470464_142470466del , CM000665.2:g.142470464_142470466del	GRCh38
NC_000003.11:g.142189306_142189308del , CM000665.1:g.142189306_142189308del	GRCh37
NC_000003.10:g.143671996_143671998del	NCBI36
NG_008951.1:g.113364_113366del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-280_6222-278del MANE Select	ENSP00000343741.4:n.6222-280_6222-278del
ENST00000513291.2:n.1406-280_1406-278del
ENST00000654170.1:n.1065-280_1065-278del
ENST00000656590.1:c.5012-280_5012-278del
ENST00000661310.1:c.6030-280_6030-278del	ENSP00000499589.1:n.6030-280_6030-278del
ENST00000665483.1:n.77-280_77-278del
ENST00000666447.1:n.57-280_57-278del
ENST00000666943.1:n.1686-280_1686-278del
ENST00000350721.8:c.6222-280_6222-278del	ENSP00000343741.4:n.6222-280_6222-278del
NM_001184.3:c.6222-280_6222-278del	NP_001175.2:n.6222-280_6222-278del
XM_011512924.1:c.6228-280_6228-278del	XP_011511226.1:n.6228-280_6228-278del
XM_011512925.1:c.6036-280_6036-278del	XP_011511227.1:n.6036-280_6036-278del
XR_924147.1:n.6317-280_6317-278del
XR_924148.1:n.6317-280_6317-278del
XR_924149.1:n.6196-280_6196-278del
NM_001354579.1:c.6030-280_6030-278del	NP_001341508.1:n.6030-280_6030-278del
XR_001740179.2:n.6311-280_6311-278del
XR_001740180.2:n.6365-280_6365-278del
XR_001740181.2:n.6244-280_6244-278del
XR_001740182.1:n.6196-280_6196-278del
XR_002959543.1:n.6421-280_6421-278del
XR_924148.2:n.6317-280_6317-278del
NM_001184.4:c.6222-280_6222-278del MANE Select	NP_001175.2:n.6222-280_6222-278del
NM_001354579.2:c.6030-280_6030-278del	NP_001341508.1:n.6030-280_6030-278del