Canonical Allele Identifier: CA2668018319
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553445_142553458dup , CM000665.2:g.142553445_142553458dup GRCh38
NC_000003.11:g.142272287_142272300dup , CM000665.1:g.142272287_142272300dup GRCh37
NC_000003.10:g.143754977_143754990dup NCBI36
NG_008951.1:g.30380_30393dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2634-49_2634-36dup MANE Select ENSP00000343741.4:n.2634-49_2634-36dup
ENST00000515149.3:c.*1408-49_*1408-36dup ENSP00000425897.3:n.*1408-49_*1408-36dup
ENST00000653868.1:n.2663-49_2663-36dup
ENST00000656590.1:c.1424-49_1424-36dup
ENST00000659195.1:n.5509-49_5509-36dup
ENST00000661310.1:c.2442-49_2442-36dup ENSP00000499589.1:n.2442-49_2442-36dup
ENST00000350721.8:c.2634-49_2634-36dup ENSP00000343741.4:n.2634-49_2634-36dup
NM_001184.3:c.2634-49_2634-36dup NP_001175.2:n.2634-49_2634-36dup
XM_011512924.1:c.2634-49_2634-36dup XP_011511226.1:n.2634-49_2634-36dup
XM_011512925.1:c.2442-49_2442-36dup XP_011511227.1:n.2442-49_2442-36dup
XM_011512926.1:c.2634-49_2634-36dup XP_011511228.1:n.2634-49_2634-36dup
XM_011512927.1:c.2634-49_2634-36dup XP_011511229.1:n.2634-49_2634-36dup
XR_924147.1:n.2723-49_2723-36dup
XR_924148.1:n.2723-49_2723-36dup
XR_924149.1:n.2723-49_2723-36dup
NM_001354579.1:c.2442-49_2442-36dup NP_001341508.1:n.2442-49_2442-36dup
XR_001740179.2:n.2723-49_2723-36dup
XR_001740180.2:n.2723-49_2723-36dup
XR_001740181.2:n.2723-49_2723-36dup
XR_001740182.1:n.2723-49_2723-36dup
XR_002959543.1:n.2723-49_2723-36dup
XR_924148.2:n.2723-49_2723-36dup
NM_001184.4:c.2634-49_2634-36dup MANE Select NP_001175.2:n.2634-49_2634-36dup
NM_001354579.2:c.2442-49_2442-36dup NP_001341508.1:n.2442-49_2442-36dup