Canonical Allele Identifier: CA899909135

Gene: ATR

Linked Data

• dbSNP Id: rs1196973862
• gnomAD v3: 3-142553527-C-CA
• gnomAD v4: 3-142553527-C-CA
• MyVariant Identifiers: chr3:g.142272369_142272370insA (hg19) ; chr3:g.142553527_142553528insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553528dup , CM000665.2:g.142553528dup	GRCh38
NC_000003.11:g.142272370dup , CM000665.1:g.142272370dup	GRCh37
NC_000003.10:g.143755060dup	NCBI36
NG_008951.1:g.30299dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2633+112dup MANE Select	ENSP00000343741.4:n.2633+112dup
ENST00000515149.3:c.*1407+112dup	ENSP00000425897.3:n.*1407+112dup
ENST00000653868.1:n.2662+112dup
ENST00000656590.1:c.1423+112dup
ENST00000659195.1:n.5508+112dup
ENST00000661310.1:c.2441+112dup	ENSP00000499589.1:n.2441+112dup
ENST00000350721.8:c.2633+112dup	ENSP00000343741.4:n.2633+112dup
NM_001184.3:c.2633+112dup	NP_001175.2:n.2633+112dup
XM_011512924.1:c.2633+112dup	XP_011511226.1:n.2633+112dup
XM_011512925.1:c.2441+112dup	XP_011511227.1:n.2441+112dup
XM_011512926.1:c.2633+112dup	XP_011511228.1:n.2633+112dup
XM_011512927.1:c.2633+112dup	XP_011511229.1:n.2633+112dup
XR_924147.1:n.2722+112dup
XR_924148.1:n.2722+112dup
XR_924149.1:n.2722+112dup
NM_001354579.1:c.2441+112dup	NP_001341508.1:n.2441+112dup
XR_001740179.2:n.2722+112dup
XR_001740180.2:n.2722+112dup
XR_001740181.2:n.2722+112dup
XR_001740182.1:n.2722+112dup
XR_002959543.1:n.2722+112dup
XR_924148.2:n.2722+112dup
NM_001184.4:c.2633+112dup MANE Select	NP_001175.2:n.2633+112dup
NM_001354579.2:c.2441+112dup	NP_001341508.1:n.2441+112dup