Canonical Allele Identifier: CA1407029705

Gene: ATR

Linked Data

• dbSNP Id: rs2034566121

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.142553811_142553816del , CM000665.2:g.142553811_142553816del	GRCh38
NC_000003.11:g.142272653_142272658del , CM000665.1:g.142272653_142272658del	GRCh37
NC_000003.10:g.143755343_143755348del	NCBI36
NG_008951.1:g.30016_30021del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350721.9:c.2532+14_2532+19del MANE Select	ENSP00000343741.4:n.2532+14_2532+19del
ENST00000515149.3:c.*1306+14_*1306+19del	ENSP00000425897.3:n.*1306+14_*1306+19del
ENST00000653868.1:n.2561+14_2561+19del
ENST00000656590.1:c.1322+14_1322+19del
ENST00000659195.1:n.5407+14_5407+19del
ENST00000661310.1:c.2340+14_2340+19del	ENSP00000499589.1:n.2340+14_2340+19del
ENST00000350721.8:c.2532+14_2532+19del	ENSP00000343741.4:n.2532+14_2532+19del
NM_001184.3:c.2532+14_2532+19del	NP_001175.2:n.2532+14_2532+19del
XM_011512924.1:c.2532+14_2532+19del	XP_011511226.1:n.2532+14_2532+19del
XM_011512925.1:c.2340+14_2340+19del	XP_011511227.1:n.2340+14_2340+19del
XM_011512926.1:c.2532+14_2532+19del	XP_011511228.1:n.2532+14_2532+19del
XM_011512927.1:c.2532+14_2532+19del	XP_011511229.1:n.2532+14_2532+19del
XR_924147.1:n.2621+14_2621+19del
XR_924148.1:n.2621+14_2621+19del
XR_924149.1:n.2621+14_2621+19del
NM_001354579.1:c.2340+14_2340+19del	NP_001341508.1:n.2340+14_2340+19del
XR_001740179.2:n.2621+14_2621+19del
XR_001740180.2:n.2621+14_2621+19del
XR_001740181.2:n.2621+14_2621+19del
XR_001740182.1:n.2621+14_2621+19del
XR_002959543.1:n.2621+14_2621+19del
XR_924148.2:n.2621+14_2621+19del
NM_001184.4:c.2532+14_2532+19del MANE Select	NP_001175.2:n.2532+14_2532+19del
NM_001354579.2:c.2340+14_2340+19del	NP_001341508.1:n.2340+14_2340+19del