Canonical Allele Identifier: CA1054353944

Gene: ATR

Linked Data

• dbSNP Id: rs2071223035
• gnomAD v3: 3-142470012-TG-T
• gnomAD v4: 3-142470012-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470013del , CM000665.2:g.142470013del	GRCh38
NC_000003.11:g.142188855del , CM000665.1:g.142188855del	GRCh37
NC_000003.10:g.143671545del	NCBI36
NG_008951.1:g.113814del

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+73del MANE Select	ENSP00000343741.4:n.6319+73del
ENST00000513291.2:n.1503+73del
ENST00000654170.1:n.1162+73del
ENST00000656590.1:c.5109+73del
ENST00000661310.1:c.6127+73del	ENSP00000499589.1:n.6127+73del
ENST00000665483.1:n.174+73del
ENST00000666447.1:n.154+73del
ENST00000666943.1:n.1783+73del
ENST00000350721.8:c.6319+73del	ENSP00000343741.4:n.6319+73del
NM_001184.3:c.6319+73del	NP_001175.2:n.6319+73del
XM_011512924.1:c.6325+73del	XP_011511226.1:n.6325+73del
XM_011512925.1:c.6133+73del	XP_011511227.1:n.6133+73del
XR_924147.1:n.6414+73del
XR_924148.1:n.6414+73del
XR_924149.1:n.6293+73del
NM_001354579.1:c.6127+73del	NP_001341508.1:n.6127+73del
XR_001740179.2:n.6408+73del
XR_001740180.2:n.6462+73del
XR_001740181.2:n.6341+73del
XR_001740182.1:n.6293+73del
XR_002959543.1:n.6518+73del
XR_924148.2:n.6414+73del
NM_001184.4:c.6319+73del MANE Select	NP_001175.2:n.6319+73del
NM_001354579.2:c.6127+73del	NP_001341508.1:n.6127+73del