Canonical Allele Identifier: CA2513567820
Gene: ATR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553740_142553741insT , CM000665.2:g.142553740_142553741insT GRCh38
NC_000003.11:g.142272582_142272583insT , CM000665.1:g.142272582_142272583insT GRCh37
NC_000003.10:g.143755272_143755273insT NCBI36
NG_008951.1:g.30086_30087insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2533-1_2533insA MANE Select ENSP00000343741.4:n.2533-1_2533insA
ENST00000515149.3:c.*1307-1_*1307insA ENSP00000425897.3:n.*1307-1_*1307insA
ENST00000653868.1:n.2562-1_2562insA
ENST00000656590.1:c.1323-1_1323insA
ENST00000659195.1:n.5408-1_5408insA
ENST00000661310.1:c.2341-1_2341insA ENSP00000499589.1:n.2341-1_2341insA
ENST00000350721.8:c.2533-1_2533insA ENSP00000343741.4:n.2533-1_2533insA
NM_001184.3:c.2533-1_2533insA NP_001175.2:n.2533-1_2533insA
XM_011512924.1:c.2533-1_2533insA XP_011511226.1:n.2533-1_2533insA
XM_011512925.1:c.2341-1_2341insA XP_011511227.1:n.2341-1_2341insA
XM_011512926.1:c.2533-1_2533insA XP_011511228.1:n.2533-1_2533insA
XM_011512927.1:c.2533-1_2533insA XP_011511229.1:n.2533-1_2533insA
XR_924147.1:n.2622-1_2622insA
XR_924148.1:n.2622-1_2622insA
XR_924149.1:n.2622-1_2622insA
NM_001354579.1:c.2341-1_2341insA NP_001341508.1:n.2341-1_2341insA
XR_001740179.2:n.2622-1_2622insA
XR_001740180.2:n.2622-1_2622insA
XR_001740181.2:n.2622-1_2622insA
XR_001740182.1:n.2622-1_2622insA
XR_002959543.1:n.2622-1_2622insA
XR_924148.2:n.2622-1_2622insA
NM_001184.4:c.2533-1_2533insA MANE Select NP_001175.2:n.2533-1_2533insA
NM_001354579.2:c.2341-1_2341insA NP_001341508.1:n.2341-1_2341insA