Canonical Allele Identifier: CA899908961

Gene: ATR

Linked Data

• dbSNP Id: rs142950892
• MyVariant Identifiers: chr3:g.142272275_142272276insCA (hg19) ; chr3:g.142553433_142553434insCA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553433_142553434insCA , CM000665.2:g.142553433_142553434insCA	GRCh38
NC_000003.11:g.142272275_142272276insCA , CM000665.1:g.142272275_142272276insCA	GRCh37
NC_000003.10:g.143754965_143754966insCA	NCBI36
NG_008951.1:g.30394_30395insGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2634-35_2634-34insGT MANE Select	ENSP00000343741.4:n.2634-35_2634-34insGT
ENST00000515149.3:c.*1408-35_*1408-34insGT	ENSP00000425897.3:n.*1408-35_*1408-34insGT
ENST00000653868.1:n.2663-35_2663-34insGT
ENST00000656590.1:c.1424-35_1424-34insGT
ENST00000659195.1:n.5509-35_5509-34insGT
ENST00000661310.1:c.2442-35_2442-34insGT	ENSP00000499589.1:n.2442-35_2442-34insGT
ENST00000350721.8:c.2634-35_2634-34insGT	ENSP00000343741.4:n.2634-35_2634-34insGT
NM_001184.3:c.2634-35_2634-34insGT	NP_001175.2:n.2634-35_2634-34insGT
XM_011512924.1:c.2634-35_2634-34insGT	XP_011511226.1:n.2634-35_2634-34insGT
XM_011512925.1:c.2442-35_2442-34insGT	XP_011511227.1:n.2442-35_2442-34insGT
XM_011512926.1:c.2634-35_2634-34insGT	XP_011511228.1:n.2634-35_2634-34insGT
XM_011512927.1:c.2634-35_2634-34insGT	XP_011511229.1:n.2634-35_2634-34insGT
XR_924147.1:n.2723-35_2723-34insGT
XR_924148.1:n.2723-35_2723-34insGT
XR_924149.1:n.2723-35_2723-34insGT
NM_001354579.1:c.2442-35_2442-34insGT	NP_001341508.1:n.2442-35_2442-34insGT
XR_001740179.2:n.2723-35_2723-34insGT
XR_001740180.2:n.2723-35_2723-34insGT
XR_001740181.2:n.2723-35_2723-34insGT
XR_001740182.1:n.2723-35_2723-34insGT
XR_002959543.1:n.2723-35_2723-34insGT
XR_924148.2:n.2723-35_2723-34insGT
NM_001184.4:c.2634-35_2634-34insGT MANE Select	NP_001175.2:n.2634-35_2634-34insGT
NM_001354579.2:c.2442-35_2442-34insGT	NP_001341508.1:n.2442-35_2442-34insGT