Canonical Allele Identifier: CA10603286
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 280663
ClinVar RCV Id: RCV000315218
dbSNP Id: rs886041829
MyVariant Identifiers: chr16:g.89348575_89348578del (hg19) chr16:g.89282167_89282170del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89282168_89282171del , CM000678.2:g.89282168_89282171del GRCh38
NC_000016.9:g.89348576_89348579del , CM000678.1:g.89348576_89348579del GRCh37
NC_000016.8:g.87876077_87876080del NCBI36
NG_032003.1:g.213392_213395del
NG_032003.2:g.213392_213395del

Transcript Alleles

HGVS Amino-acid change
ENST00000301030.10:c.4372_4375del MANE Select ENSP00000301030.4:p.Glu1458ArgfsTer?
ENST00000330736.10:c.*4175_*4178del ENSP00000330815.5:n.*4175_*4178del
ENST00000378330.7:c.4372_4375del ENSP00000367581.2:p.Glu1458ArgfsTer?
ENST00000642600.1:c.4372_4375del ENSP00000495226.1:p.Glu1458ArgfsTer?
ENST00000644285.1:c.744+6358_744+6361del ENSP00000496476.1:n.744+6358_744+6361del
ENST00000301030.8:c.4372_4375del ENSP00000301030.4:p.Glu1458ArgfsTer?
ENST00000330736.9:c.*4175_*4178del ENSP00000330815.5:n.*4175_*4178del
ENST00000378330.6:c.4372_4375del ENSP00000367581.2:p.Glu1458ArgfsTer?
ENST00000562194.1:c.151+6358_151+6361del
NM_001256182.1:c.4372_4375del NP_001243111.1:p.Glu1458ArgfsTer?
NM_001256183.1:c.4372_4375del NP_001243112.1:p.Glu1458ArgfsTer?
NM_013275.5:c.4372_4375del NP_037407.4:p.Glu1458ArgfsTer?
XM_006721181.1:c.4270_4273del XP_006721244.1:p.Glu1424ArgfsTer?
XM_006721184.2:c.4075_4078del XP_006721247.1:p.Glu1359ArgfsTer?
XM_011523051.1:c.4372_4375del XP_011521353.1:p.Glu1458ArgfsTer?
XM_011523052.1:c.4372_4375del XP_011521354.1:p.Glu1458ArgfsTer?
XM_011523053.1:c.4372_4375del XP_011521355.1:p.Glu1458ArgfsTer?
XM_011523054.1:c.4270_4273del XP_011521356.1:p.Glu1424ArgfsTer?
XM_011523055.1:c.4270_4273del XP_011521357.1:p.Glu1424ArgfsTer?
XM_011523056.1:c.4243_4246del XP_011521358.1:p.Glu1415ArgfsTer?
XM_011523057.1:c.4372_4375del XP_011521359.1:p.Glu1458ArgfsTer?
XM_011523051.3:c.4372_4375del XP_011521353.1:p.Glu1458ArgfsTer?
XM_011523053.2:c.4372_4375del XP_011521355.1:p.Glu1458ArgfsTer?
XM_011523054.2:c.4270_4273del XP_011521356.1:p.Glu1424ArgfsTer?
XM_011523055.2:c.4270_4273del XP_011521357.1:p.Glu1424ArgfsTer?
XM_011523056.2:c.4243_4246del XP_011521358.1:p.Glu1415ArgfsTer?
XM_011523057.2:c.4372_4375del XP_011521359.1:p.Glu1458ArgfsTer?
XM_017023182.2:c.4372_4375del XP_016878671.1:p.Glu1458ArgfsTer?
XM_017023183.1:c.4372_4375del XP_016878672.1:p.Glu1458ArgfsTer?
XM_017023184.1:c.4372_4375del XP_016878673.1:p.Glu1458ArgfsTer?
XM_017023185.1:c.4372_4375del XP_016878674.1:p.Glu1458ArgfsTer?
XM_017023186.1:c.4372_4375del XP_016878675.1:p.Glu1458ArgfsTer?
XM_017023187.1:c.4372_4375del XP_016878676.1:p.Glu1458ArgfsTer?
XM_024450244.1:c.4270_4273del XP_024306012.1:p.Glu1424ArgfsTer?
NM_013275.6:c.4372_4375del MANE Select NP_037407.4:p.Glu1458ArgfsTer?
NM_001256182.2:c.4372_4375del NP_001243111.1:p.Glu1458ArgfsTer?
NM_001256183.2:c.4372_4375del NP_001243112.1:p.Glu1458ArgfsTer?
Search 100 bp 5'
Search 100 bp 3'