Canonical Allele Identifier: CA2668039283

Gene: ATR

Linked Data

• gnomAD v4: 3-142470081-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142470081_142470082insGG , CM000665.2:g.142470081_142470082insGG	GRCh38
NC_000003.11:g.142188923_142188924insGG , CM000665.1:g.142188923_142188924insGG	GRCh37
NC_000003.10:g.143671613_143671614insGG	NCBI36
NG_008951.1:g.113745_113746insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000350721.9:c.6319+4_6319+5insCC MANE Select	ENSP00000343741.4:n.6319+4_6319+5insCC
ENST00000513291.2:n.1503+4_1503+5insCC
ENST00000654170.1:n.1162+4_1162+5insCC
ENST00000656590.1:c.5109+4_5109+5insCC
ENST00000661310.1:c.6127+4_6127+5insCC	ENSP00000499589.1:n.6127+4_6127+5insCC
ENST00000665483.1:n.174+4_174+5insCC
ENST00000666447.1:n.154+4_154+5insCC
ENST00000666943.1:n.1783+4_1783+5insCC
ENST00000350721.8:c.6319+4_6319+5insCC	ENSP00000343741.4:n.6319+4_6319+5insCC
NM_001184.3:c.6319+4_6319+5insCC	NP_001175.2:n.6319+4_6319+5insCC
XM_011512924.1:c.6325+4_6325+5insCC	XP_011511226.1:n.6325+4_6325+5insCC
XM_011512925.1:c.6133+4_6133+5insCC	XP_011511227.1:n.6133+4_6133+5insCC
XR_924147.1:n.6414+4_6414+5insCC
XR_924148.1:n.6414+4_6414+5insCC
XR_924149.1:n.6293+4_6293+5insCC
NM_001354579.1:c.6127+4_6127+5insCC	NP_001341508.1:n.6127+4_6127+5insCC
XR_001740179.2:n.6408+4_6408+5insCC
XR_001740180.2:n.6462+4_6462+5insCC
XR_001740181.2:n.6341+4_6341+5insCC
XR_001740182.1:n.6293+4_6293+5insCC
XR_002959543.1:n.6518+4_6518+5insCC
XR_924148.2:n.6414+4_6414+5insCC
NM_001184.4:c.6319+4_6319+5insCC MANE Select	NP_001175.2:n.6319+4_6319+5insCC
NM_001354579.2:c.6127+4_6127+5insCC	NP_001341508.1:n.6127+4_6127+5insCC