Canonical Allele Identifier: CA2668018347

Gene: ATR

Linked Data

• gnomAD v4: 3-142553435-C-CAA

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553436_142553437insAA , CM000665.2:g.142553436_142553437insAA	GRCh38
NC_000003.11:g.142272278_142272279insAA , CM000665.1:g.142272278_142272279insAA	GRCh37
NC_000003.10:g.143754968_143754969insAA	NCBI36
NG_008951.1:g.30391_30392insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2634-38_2634-37insTT MANE Select	ENSP00000343741.4:n.2634-38_2634-37insTT
ENST00000515149.3:c.*1408-38_*1408-37insTT	ENSP00000425897.3:n.*1408-38_*1408-37insTT
ENST00000653868.1:n.2663-38_2663-37insTT
ENST00000656590.1:c.1424-38_1424-37insTT
ENST00000659195.1:n.5509-38_5509-37insTT
ENST00000661310.1:c.2442-38_2442-37insTT	ENSP00000499589.1:n.2442-38_2442-37insTT
ENST00000350721.8:c.2634-38_2634-37insTT	ENSP00000343741.4:n.2634-38_2634-37insTT
NM_001184.3:c.2634-38_2634-37insTT	NP_001175.2:n.2634-38_2634-37insTT
XM_011512924.1:c.2634-38_2634-37insTT	XP_011511226.1:n.2634-38_2634-37insTT
XM_011512925.1:c.2442-38_2442-37insTT	XP_011511227.1:n.2442-38_2442-37insTT
XM_011512926.1:c.2634-38_2634-37insTT	XP_011511228.1:n.2634-38_2634-37insTT
XM_011512927.1:c.2634-38_2634-37insTT	XP_011511229.1:n.2634-38_2634-37insTT
XR_924147.1:n.2723-38_2723-37insTT
XR_924148.1:n.2723-38_2723-37insTT
XR_924149.1:n.2723-38_2723-37insTT
NM_001354579.1:c.2442-38_2442-37insTT	NP_001341508.1:n.2442-38_2442-37insTT
XR_001740179.2:n.2723-38_2723-37insTT
XR_001740180.2:n.2723-38_2723-37insTT
XR_001740181.2:n.2723-38_2723-37insTT
XR_001740182.1:n.2723-38_2723-37insTT
XR_002959543.1:n.2723-38_2723-37insTT
XR_924148.2:n.2723-38_2723-37insTT
NM_001184.4:c.2634-38_2634-37insTT MANE Select	NP_001175.2:n.2634-38_2634-37insTT
NM_001354579.2:c.2442-38_2442-37insTT	NP_001341508.1:n.2442-38_2442-37insTT