Canonical Allele Identifier: CA2668018376
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553444_142553445insTA , CM000665.2:g.142553444_142553445insTA GRCh38
NC_000003.11:g.142272286_142272287insTA , CM000665.1:g.142272286_142272287insTA GRCh37
NC_000003.10:g.143754976_143754977insTA NCBI36
NG_008951.1:g.30383_30384insAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2634-46_2634-45insAT MANE Select ENSP00000343741.4:n.2634-46_2634-45insAT
ENST00000515149.3:c.*1408-46_*1408-45insAT ENSP00000425897.3:n.*1408-46_*1408-45insAT
ENST00000653868.1:n.2663-46_2663-45insAT
ENST00000656590.1:c.1424-46_1424-45insAT
ENST00000659195.1:n.5509-46_5509-45insAT
ENST00000661310.1:c.2442-46_2442-45insAT ENSP00000499589.1:n.2442-46_2442-45insAT
ENST00000350721.8:c.2634-46_2634-45insAT ENSP00000343741.4:n.2634-46_2634-45insAT
NM_001184.3:c.2634-46_2634-45insAT NP_001175.2:n.2634-46_2634-45insAT
XM_011512924.1:c.2634-46_2634-45insAT XP_011511226.1:n.2634-46_2634-45insAT
XM_011512925.1:c.2442-46_2442-45insAT XP_011511227.1:n.2442-46_2442-45insAT
XM_011512926.1:c.2634-46_2634-45insAT XP_011511228.1:n.2634-46_2634-45insAT
XM_011512927.1:c.2634-46_2634-45insAT XP_011511229.1:n.2634-46_2634-45insAT
XR_924147.1:n.2723-46_2723-45insAT
XR_924148.1:n.2723-46_2723-45insAT
XR_924149.1:n.2723-46_2723-45insAT
NM_001354579.1:c.2442-46_2442-45insAT NP_001341508.1:n.2442-46_2442-45insAT
XR_001740179.2:n.2723-46_2723-45insAT
XR_001740180.2:n.2723-46_2723-45insAT
XR_001740181.2:n.2723-46_2723-45insAT
XR_001740182.1:n.2723-46_2723-45insAT
XR_002959543.1:n.2723-46_2723-45insAT
XR_924148.2:n.2723-46_2723-45insAT
NM_001184.4:c.2634-46_2634-45insAT MANE Select NP_001175.2:n.2634-46_2634-45insAT
NM_001354579.2:c.2442-46_2442-45insAT NP_001341508.1:n.2442-46_2442-45insAT