Canonical Allele Identifier: CA2668039287

Gene: ATR

Linked Data

• gnomAD v4: 3-142470155-AT-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470156del , CM000665.2:g.142470156del	GRCh38
NC_000003.11:g.142188998del , CM000665.1:g.142188998del	GRCh37
NC_000003.10:g.143671688del	NCBI36
NG_008951.1:g.113671del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.6249del MANE Select	ENSP00000343741.4:p.Tyr2084IlefsTer8
ENST00000513291.2:n.1433del
ENST00000654170.1:n.1092del
ENST00000656590.1:c.5039del
ENST00000661310.1:c.6057del	ENSP00000499589.1:p.Tyr2020IlefsTer8
ENST00000665483.1:n.104del
ENST00000666447.1:n.84del
ENST00000666943.1:n.1713del
ENST00000350721.8:c.6249del	ENSP00000343741.4:p.Tyr2084IlefsTer8
NM_001184.3:c.6249del	NP_001175.2:p.Tyr2084IlefsTer8
XM_011512924.1:c.6255del	XP_011511226.1:p.Tyr2086IlefsTer8
XM_011512925.1:c.6063del	XP_011511227.1:p.Tyr2022IlefsTer8
XR_924147.1:n.6344del
XR_924148.1:n.6344del
XR_924149.1:n.6223del
NM_001354579.1:c.6057del	NP_001341508.1:p.Tyr2020IlefsTer8
XR_001740179.2:n.6338del
XR_001740180.2:n.6392del
XR_001740181.2:n.6271del
XR_001740182.1:n.6223del
XR_002959543.1:n.6448del
XR_924148.2:n.6344del
NM_001184.4:c.6249del MANE Select	NP_001175.2:p.Tyr2084IlefsTer8
NM_001354579.2:c.6057del	NP_001341508.1:p.Tyr2020IlefsTer8