Canonical Allele Identifier: CA84756194

Gene: ATR

Linked Data

• dbSNP Id: rs977966828
• gnomAD v4: 3-142563118-TAAAC-T
• MyVariant Identifiers: chr3:g.142281961_142281964del (hg19) ; chr3:g.142563119_142563122del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142563122_142563125del , CM000665.2:g.142563122_142563125del	GRCh38
NC_000003.11:g.142281964_142281967del , CM000665.1:g.142281964_142281967del	GRCh37
NC_000003.10:g.143764654_143764657del	NCBI36
NG_008951.1:g.20705_20708del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.293-13_293-10del MANE Select	ENSP00000343741.4:n.293-13_293-10del
ENST00000515149.3:c.293-1701_293-1698del	ENSP00000425897.3:n.293-1701_293-1698del
ENST00000653868.1:n.322-13_322-10del
ENST00000657914.1:n.2638_2641del
ENST00000659195.1:n.2345_2348del
ENST00000661310.1:c.293-13_293-10del	ENSP00000499589.1:n.293-13_293-10del
ENST00000350721.8:c.293-13_293-10del	ENSP00000343741.4:n.293-13_293-10del
ENST00000507148.1:c.293-774_293-771del	ENSP00000426595.1:n.293-774_293-771del
NM_001184.3:c.293-13_293-10del	NP_001175.2:n.293-13_293-10del
XM_011512924.1:c.293-13_293-10del	XP_011511226.1:n.293-13_293-10del
XM_011512925.1:c.293-13_293-10del	XP_011511227.1:n.293-13_293-10del
XM_011512926.1:c.293-13_293-10del	XP_011511228.1:n.293-13_293-10del
XM_011512927.1:c.293-13_293-10del	XP_011511229.1:n.293-13_293-10del
XR_924147.1:n.382-13_382-10del
XR_924148.1:n.382-13_382-10del
XR_924149.1:n.382-13_382-10del
NM_001354579.1:c.293-13_293-10del	NP_001341508.1:n.293-13_293-10del
XR_001740179.2:n.382-13_382-10del
XR_001740180.2:n.382-13_382-10del
XR_001740181.2:n.382-13_382-10del
XR_001740182.1:n.382-13_382-10del
XR_002959543.1:n.382-13_382-10del
XR_924148.2:n.382-13_382-10del
NM_001184.4:c.293-13_293-10del MANE Select	NP_001175.2:n.293-13_293-10del
NM_001354579.2:c.293-13_293-10del	NP_001341508.1:n.293-13_293-10del