Canonical Allele Identifier: CA2527528233

Gene: ATR

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470333_142470334del , CM000665.2:g.142470333_142470334del	GRCh38
NC_000003.11:g.142189175_142189176del , CM000665.1:g.142189175_142189176del	GRCh37
NC_000003.10:g.143671865_143671866del	NCBI36
NG_008951.1:g.113494_113495del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-150_6222-149del MANE Select	ENSP00000343741.4:n.6222-150_6222-149del
ENST00000513291.2:n.1406-150_1406-149del
ENST00000654170.1:n.1065-150_1065-149del
ENST00000656590.1:c.5012-150_5012-149del
ENST00000661310.1:c.6030-150_6030-149del	ENSP00000499589.1:n.6030-150_6030-149del
ENST00000665483.1:n.77-150_77-149del
ENST00000666447.1:n.57-150_57-149del
ENST00000666943.1:n.1686-150_1686-149del
ENST00000350721.8:c.6222-150_6222-149del	ENSP00000343741.4:n.6222-150_6222-149del
NM_001184.3:c.6222-150_6222-149del	NP_001175.2:n.6222-150_6222-149del
XM_011512924.1:c.6228-150_6228-149del	XP_011511226.1:n.6228-150_6228-149del
XM_011512925.1:c.6036-150_6036-149del	XP_011511227.1:n.6036-150_6036-149del
XR_924147.1:n.6317-150_6317-149del
XR_924148.1:n.6317-150_6317-149del
XR_924149.1:n.6196-150_6196-149del
NM_001354579.1:c.6030-150_6030-149del	NP_001341508.1:n.6030-150_6030-149del
XR_001740179.2:n.6311-150_6311-149del
XR_001740180.2:n.6365-150_6365-149del
XR_001740181.2:n.6244-150_6244-149del
XR_001740182.1:n.6196-150_6196-149del
XR_002959543.1:n.6421-150_6421-149del
XR_924148.2:n.6317-150_6317-149del
NM_001184.4:c.6222-150_6222-149del MANE Select	NP_001175.2:n.6222-150_6222-149del
NM_001354579.2:c.6030-150_6030-149del	NP_001341508.1:n.6030-150_6030-149del