Canonical Allele Identifier: CA2668018569

Gene: ATR

Linked Data

• gnomAD v4: 3-142553529-CATTT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553530_142553533del , CM000665.2:g.142553530_142553533del	GRCh38
NC_000003.11:g.142272372_142272375del , CM000665.1:g.142272372_142272375del	GRCh37
NC_000003.10:g.143755062_143755065del	NCBI36
NG_008951.1:g.30294_30297del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2633+107_2633+110del MANE Select	ENSP00000343741.4:n.2633+107_2633+110del
ENST00000515149.3:c.*1407+107_*1407+110del	ENSP00000425897.3:n.*1407+107_*1407+110del
ENST00000653868.1:n.2662+107_2662+110del
ENST00000656590.1:c.1423+107_1423+110del
ENST00000659195.1:n.5508+107_5508+110del
ENST00000661310.1:c.2441+107_2441+110del	ENSP00000499589.1:n.2441+107_2441+110del
ENST00000350721.8:c.2633+107_2633+110del	ENSP00000343741.4:n.2633+107_2633+110del
NM_001184.3:c.2633+107_2633+110del	NP_001175.2:n.2633+107_2633+110del
XM_011512924.1:c.2633+107_2633+110del	XP_011511226.1:n.2633+107_2633+110del
XM_011512925.1:c.2441+107_2441+110del	XP_011511227.1:n.2441+107_2441+110del
XM_011512926.1:c.2633+107_2633+110del	XP_011511228.1:n.2633+107_2633+110del
XM_011512927.1:c.2633+107_2633+110del	XP_011511229.1:n.2633+107_2633+110del
XR_924147.1:n.2722+107_2722+110del
XR_924148.1:n.2722+107_2722+110del
XR_924149.1:n.2722+107_2722+110del
NM_001354579.1:c.2441+107_2441+110del	NP_001341508.1:n.2441+107_2441+110del
XR_001740179.2:n.2722+107_2722+110del
XR_001740180.2:n.2722+107_2722+110del
XR_001740181.2:n.2722+107_2722+110del
XR_001740182.1:n.2722+107_2722+110del
XR_002959543.1:n.2722+107_2722+110del
XR_924148.2:n.2722+107_2722+110del
NM_001184.4:c.2633+107_2633+110del MANE Select	NP_001175.2:n.2633+107_2633+110del
NM_001354579.2:c.2441+107_2441+110del	NP_001341508.1:n.2441+107_2441+110del