Canonical Allele Identifier: CA2400238970
Gene: CHEK2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.28697204_28697205delinsCA , CM000684.2:g.28697204_28697205delinsCA GRCh38
NC_000022.10:g.29093192_29093193delinsCA , CM000684.1:g.29093192_29093193delinsCA GRCh37
NC_000022.9:g.27423192_27423193delinsCA NCBI36
NG_008150.1:g.49630_49631delinsTG
NG_008150.2:g.49662_49663delinsTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000711048.1:c.1009-1963_1009-1962delinsTG ENSP00000518557.1:n.1009-1963_1009-1962delinsTG
ENST00000402731.6:c.808-218_808-217delinsTG ENSP00000384835.2:n.808-218_808-217delinsTG
ENST00000404276.6:c.1009-218_1009-217delinsTG MANE Select ENSP00000385747.1:n.1009-218_1009-217delinsTG
ENST00000425190.7:c.346-218_346-217delinsTG ENSP00000390244.2:n.346-218_346-217delinsTG
ENST00000464581.6:c.349-218_349-217delinsTG ENSP00000483777.2:n.349-218_349-217delinsTG
ENST00000648295.1:n.561-218_561-217delinsTG
ENST00000649563.1:c.346-218_346-217delinsTG ENSP00000496928.1:n.346-218_346-217delinsTG
ENST00000650281.1:c.1009-218_1009-217delinsTG ENSP00000497000.1:n.1009-218_1009-217delinsTG
ENST00000328354.10:c.1009-218_1009-217delinsTG ENSP00000329178.6:n.1009-218_1009-217delinsTG
ENST00000348295.7:c.1009-1332_1009-1331delinsTG ENSP00000329012.5:n.1009-1332_1009-1331delinsTG
ENST00000382580.6:c.1138-218_1138-217delinsTG ENSP00000372023.2:n.1138-218_1138-217delinsTG
ENST00000402731.5:c.1009-1332_1009-1331delinsTG ENSP00000384835.1:n.1009-1332_1009-1331delinsTG
ENST00000403642.5:c.736-218_736-217delinsTG ENSP00000384919.1:n.736-218_736-217delinsTG
ENST00000404276.5:c.1009-218_1009-217delinsTG ENSP00000385747.1:n.1009-218_1009-217delinsTG
ENST00000405598.5:c.1009-218_1009-217delinsTG ENSP00000386087.1:n.1009-218_1009-217delinsTG
ENST00000416671.5:c.*499-218_*499-217delinsTG ENSP00000402225.1:n.*499-218_*499-217delinsTG
ENST00000417588.5:c.918-218_918-217delinsTG ENSP00000412901.1:n.918-218_918-217delinsTG
ENST00000425190.6:c.346-218_346-217delinsTG ENSP00000390244.1:n.346-218_346-217delinsTG
ENST00000433028.6:c.*734-218_*734-217delinsTG ENSP00000403659.1:n.*734-218_*734-217delinsTG
ENST00000433728.5:c.947-218_947-217delinsTG ENSP00000404400.1:n.947-218_947-217delinsTG
ENST00000434810.5:c.240-218_240-217delinsTG
ENST00000447421.5:c.808-218_808-217delinsTG ENSP00000397478.2:n.808-218_808-217delinsTG
ENST00000448511.5:c.899-218_899-217delinsTG ENSP00000404567.1:n.899-218_899-217delinsTG
ENST00000456369.5:c.263+2633_263+2634delinsTG
ENST00000464581.5:c.349-218_349-217delinsTG ENSP00000483777.1:n.349-218_349-217delinsTG
ENST00000491919.5:n.566-218_566-217delinsTG
NM_001005735.1:c.1138-218_1138-217delinsTG NP_001005735.1:n.1138-218_1138-217delinsTG
NM_001257387.1:c.346-218_346-217delinsTG NP_001244316.1:n.346-218_346-217delinsTG
NM_007194.3:c.1009-218_1009-217delinsTG NP_009125.1:n.1009-218_1009-217delinsTG
NM_145862.2:c.1009-1332_1009-1331delinsTG NP_665861.1:n.1009-1332_1009-1331delinsTG
XM_006724114.2:c.529-218_529-217delinsTG XP_006724177.1:n.529-218_529-217delinsTG
XM_006724116.2:c.466-218_466-217delinsTG XP_006724179.2:n.466-218_466-217delinsTG
XM_011529839.1:c.1168-218_1168-217delinsTG XP_011528141.1:n.1168-218_1168-217delinsTG
XM_011529840.1:c.1168-1332_1168-1331delinsTG XP_011528142.1:n.1168-1332_1168-1331delinsTG
XM_011529841.1:c.937-218_937-217delinsTG XP_011528143.1:n.937-218_937-217delinsTG
XM_011529842.1:c.838-218_838-217delinsTG XP_011528144.1:n.838-218_838-217delinsTG
XM_011529843.1:c.808-218_808-217delinsTG XP_011528145.1:n.808-218_808-217delinsTG
XM_011529844.1:c.1168-76_1168-75delinsTG XP_011528146.1:n.1168-76_1168-75delinsTG
XM_011529845.1:c.346-218_346-217delinsTG XP_011528147.1:n.346-218_346-217delinsTG
XR_937805.1:n.1168-218_1168-217delinsTG
XR_937806.1:n.1163-1332_1163-1331delinsTG
XR_937807.1:n.1163-76_1163-75delinsTG
NM_001349956.1:c.808-218_808-217delinsTG NP_001336885.1:n.808-218_808-217delinsTG
NM_007194.4:c.1009-218_1009-217delinsTG MANE Select NP_009125.1:n.1009-218_1009-217delinsTG
XM_006724114.3:c.562-218_562-217delinsTG XP_006724177.2:n.562-218_562-217delinsTG
XM_011529839.2:c.1168-218_1168-217delinsTG XP_011528141.1:n.1168-218_1168-217delinsTG
XM_011529840.3:c.1168-1332_1168-1331delinsTG XP_011528142.1:n.1168-1332_1168-1331delinsTG
XM_011529842.2:c.838-218_838-217delinsTG XP_011528144.1:n.838-218_838-217delinsTG
XM_011529844.2:c.1168-76_1168-75delinsTG XP_011528146.1:n.1168-76_1168-75delinsTG
XM_011529845.2:c.346-218_346-217delinsTG XP_011528147.1:n.346-218_346-217delinsTG
XM_017028560.1:c.1132-218_1132-217delinsTG XP_016884049.1:n.1132-218_1132-217delinsTG
XM_017028561.2:c.346-218_346-217delinsTG XP_016884050.1:n.346-218_346-217delinsTG
XM_024452148.1:c.1039-218_1039-217delinsTG XP_024307916.1:n.1039-218_1039-217delinsTG
XM_024452149.1:c.1039-1332_1039-1331delinsTG XP_024307917.1:n.1039-1332_1039-1331delinsTG
XR_937805.2:n.1179-218_1179-217delinsTG
XR_937806.2:n.1179-1332_1179-1331delinsTG
XR_937807.2:n.1179-76_1179-75delinsTG
NM_001005735.2:c.1138-218_1138-217delinsTG NP_001005735.1:n.1138-218_1138-217delinsTG
NM_001257387.2:c.346-218_346-217delinsTG NP_001244316.1:n.346-218_346-217delinsTG
NM_001349956.2:c.808-218_808-217delinsTG NP_001336885.1:n.808-218_808-217delinsTG
Search 100 bp 5'
Search 100 bp 3'