Canonical Allele Identifier: CA2668018429
Gene: ATR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.142553458_142553459insCT , CM000665.2:g.142553458_142553459insCT GRCh38
NC_000003.11:g.142272300_142272301insCT , CM000665.1:g.142272300_142272301insCT GRCh37
NC_000003.10:g.143754990_143754991insCT NCBI36
NG_008951.1:g.30368_30369insAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000350721.9:c.2634-61_2634-60insAG MANE Select ENSP00000343741.4:n.2634-61_2634-60insAG
ENST00000515149.3:c.*1408-61_*1408-60insAG ENSP00000425897.3:n.*1408-61_*1408-60insAG
ENST00000653868.1:n.2663-61_2663-60insAG
ENST00000656590.1:c.1424-61_1424-60insAG
ENST00000659195.1:n.5509-61_5509-60insAG
ENST00000661310.1:c.2442-61_2442-60insAG ENSP00000499589.1:n.2442-61_2442-60insAG
ENST00000350721.8:c.2634-61_2634-60insAG ENSP00000343741.4:n.2634-61_2634-60insAG
NM_001184.3:c.2634-61_2634-60insAG NP_001175.2:n.2634-61_2634-60insAG
XM_011512924.1:c.2634-61_2634-60insAG XP_011511226.1:n.2634-61_2634-60insAG
XM_011512925.1:c.2442-61_2442-60insAG XP_011511227.1:n.2442-61_2442-60insAG
XM_011512926.1:c.2634-61_2634-60insAG XP_011511228.1:n.2634-61_2634-60insAG
XM_011512927.1:c.2634-61_2634-60insAG XP_011511229.1:n.2634-61_2634-60insAG
XR_924147.1:n.2723-61_2723-60insAG
XR_924148.1:n.2723-61_2723-60insAG
XR_924149.1:n.2723-61_2723-60insAG
NM_001354579.1:c.2442-61_2442-60insAG NP_001341508.1:n.2442-61_2442-60insAG
XR_001740179.2:n.2723-61_2723-60insAG
XR_001740180.2:n.2723-61_2723-60insAG
XR_001740181.2:n.2723-61_2723-60insAG
XR_001740182.1:n.2723-61_2723-60insAG
XR_002959543.1:n.2723-61_2723-60insAG
XR_924148.2:n.2723-61_2723-60insAG
NM_001184.4:c.2634-61_2634-60insAG MANE Select NP_001175.2:n.2634-61_2634-60insAG
NM_001354579.2:c.2442-61_2442-60insAG NP_001341508.1:n.2442-61_2442-60insAG