Canonical Allele Identifier: CA2668039318

Gene: ATR

Linked Data

• gnomAD v4: 3-142470261-AACT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470264_142470266del , CM000665.2:g.142470264_142470266del	GRCh38
NC_000003.11:g.142189106_142189108del , CM000665.1:g.142189106_142189108del	GRCh37
NC_000003.10:g.143671796_143671798del	NCBI36
NG_008951.1:g.113563_113565del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6222-81_6222-79del MANE Select	ENSP00000343741.4:n.6222-81_6222-79del
ENST00000513291.2:n.1406-81_1406-79del
ENST00000654170.1:n.1065-81_1065-79del
ENST00000656590.1:c.5012-81_5012-79del
ENST00000661310.1:c.6030-81_6030-79del	ENSP00000499589.1:n.6030-81_6030-79del
ENST00000665483.1:n.77-81_77-79del
ENST00000666447.1:n.57-81_57-79del
ENST00000666943.1:n.1686-81_1686-79del
ENST00000350721.8:c.6222-81_6222-79del	ENSP00000343741.4:n.6222-81_6222-79del
NM_001184.3:c.6222-81_6222-79del	NP_001175.2:n.6222-81_6222-79del
XM_011512924.1:c.6228-81_6228-79del	XP_011511226.1:n.6228-81_6228-79del
XM_011512925.1:c.6036-81_6036-79del	XP_011511227.1:n.6036-81_6036-79del
XR_924147.1:n.6317-81_6317-79del
XR_924148.1:n.6317-81_6317-79del
XR_924149.1:n.6196-81_6196-79del
NM_001354579.1:c.6030-81_6030-79del	NP_001341508.1:n.6030-81_6030-79del
XR_001740179.2:n.6311-81_6311-79del
XR_001740180.2:n.6365-81_6365-79del
XR_001740181.2:n.6244-81_6244-79del
XR_001740182.1:n.6196-81_6196-79del
XR_002959543.1:n.6421-81_6421-79del
XR_924148.2:n.6317-81_6317-79del
NM_001184.4:c.6222-81_6222-79del MANE Select	NP_001175.2:n.6222-81_6222-79del
NM_001354579.2:c.6030-81_6030-79del	NP_001341508.1:n.6030-81_6030-79del