Canonical Allele Identifier: CA2668020968

Gene: ATR

Linked Data

• gnomAD v4: 3-142562124-TTAC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142562127_142562129del , CM000665.2:g.142562127_142562129del	GRCh38
NC_000003.11:g.142280969_142280971del , CM000665.1:g.142280969_142280971del	GRCh37
NC_000003.10:g.143763659_143763661del	NCBI36
NG_008951.1:g.21700_21702del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.1170+105_1170+107del MANE Select	ENSP00000343741.4:n.1170+105_1170+107del
ENST00000515149.3:c.293-706_293-704del	ENSP00000425897.3:n.293-706_293-704del
ENST00000653868.1:n.1199+105_1199+107del
ENST00000657914.1:n.3528+105_3528+107del
ENST00000659195.1:n.3340_3342del
ENST00000661310.1:c.1170+105_1170+107del	ENSP00000499589.1:n.1170+105_1170+107del
ENST00000350721.8:c.1170+105_1170+107del	ENSP00000343741.4:n.1170+105_1170+107del
ENST00000507148.1:c.*106+105_*106+107del	ENSP00000426595.1:n.*106+105_*106+107del
ENST00000515149.2:c.213+105_213+107del	ENSP00000425897.2:n.213+105_213+107del
NM_001184.3:c.1170+105_1170+107del	NP_001175.2:n.1170+105_1170+107del
XM_011512924.1:c.1170+105_1170+107del	XP_011511226.1:n.1170+105_1170+107del
XM_011512925.1:c.1170+105_1170+107del	XP_011511227.1:n.1170+105_1170+107del
XM_011512926.1:c.1170+105_1170+107del	XP_011511228.1:n.1170+105_1170+107del
XM_011512927.1:c.1170+105_1170+107del	XP_011511229.1:n.1170+105_1170+107del
XR_924147.1:n.1259+105_1259+107del
XR_924148.1:n.1259+105_1259+107del
XR_924149.1:n.1259+105_1259+107del
NM_001354579.1:c.1170+105_1170+107del	NP_001341508.1:n.1170+105_1170+107del
XR_001740179.2:n.1259+105_1259+107del
XR_001740180.2:n.1259+105_1259+107del
XR_001740181.2:n.1259+105_1259+107del
XR_001740182.1:n.1259+105_1259+107del
XR_002959543.1:n.1259+105_1259+107del
XR_924148.2:n.1259+105_1259+107del
NM_001184.4:c.1170+105_1170+107del MANE Select	NP_001175.2:n.1170+105_1170+107del
NM_001354579.2:c.1170+105_1170+107del	NP_001341508.1:n.1170+105_1170+107del