Canonical Allele Identifier: CA250332
Gene: ANKRD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89284144_89284147del , CM000678.2:g.89284144_89284147del GRCh38
NC_000016.9:g.89350552_89350555del , CM000678.1:g.89350552_89350555del GRCh37
NC_000016.8:g.87878053_87878056del NCBI36
NG_032003.1:g.211418_211421del
NG_032003.2:g.211418_211421del

Transcript Alleles

HGVS Amino-acid Change
ENST00000301030.10:c.2398_2401del MANE Select ENSP00000301030.4:p.Glu800AsnfsTer?
ENST00000330736.10:c.*2201_*2204del ENSP00000330815.5:n.*2201_*2204del
ENST00000378330.7:c.2398_2401del ENSP00000367581.2:p.Glu800AsnfsTer?
ENST00000642443.1:c.2023_2026del ENSP00000493644.1:p.Glu675AsnfsTer?
ENST00000642600.1:c.2398_2401del ENSP00000495226.1:p.Glu800AsnfsTer?
ENST00000644285.1:c.744+4384_744+4387del ENSP00000496476.1:n.744+4384_744+4387del
ENST00000301030.8:c.2398_2401del ENSP00000301030.4:p.Glu800AsnfsTer?
ENST00000330736.9:c.*2201_*2204del ENSP00000330815.5:n.*2201_*2204del
ENST00000378330.6:c.2398_2401del ENSP00000367581.2:p.Glu800AsnfsTer?
ENST00000562194.1:c.151+4384_151+4387del
NM_001256182.1:c.2398_2401del NP_001243111.1:p.Glu800AsnfsTer?
NM_001256183.1:c.2398_2401del NP_001243112.1:p.Glu800AsnfsTer?
NM_013275.5:c.2398_2401del NP_037407.4:p.Glu800AsnfsTer?
XM_006721181.1:c.2296_2299del XP_006721244.1:p.Glu766AsnfsTer?
XM_006721184.2:c.2101_2104del XP_006721247.1:p.Glu701AsnfsTer?
XM_011523051.1:c.2398_2401del XP_011521353.1:p.Glu800AsnfsTer?
XM_011523052.1:c.2398_2401del XP_011521354.1:p.Glu800AsnfsTer?
XM_011523053.1:c.2398_2401del XP_011521355.1:p.Glu800AsnfsTer?
XM_011523054.1:c.2296_2299del XP_011521356.1:p.Glu766AsnfsTer?
XM_011523055.1:c.2296_2299del XP_011521357.1:p.Glu766AsnfsTer?
XM_011523056.1:c.2269_2272del XP_011521358.1:p.Glu757AsnfsTer?
XM_011523057.1:c.2398_2401del XP_011521359.1:p.Glu800AsnfsTer?
XM_011523051.3:c.2398_2401del XP_011521353.1:p.Glu800AsnfsTer?
XM_011523053.2:c.2398_2401del XP_011521355.1:p.Glu800AsnfsTer?
XM_011523054.2:c.2296_2299del XP_011521356.1:p.Glu766AsnfsTer?
XM_011523055.2:c.2296_2299del XP_011521357.1:p.Glu766AsnfsTer?
XM_011523056.2:c.2269_2272del XP_011521358.1:p.Glu757AsnfsTer?
XM_011523057.2:c.2398_2401del XP_011521359.1:p.Glu800AsnfsTer?
XM_017023182.2:c.2398_2401del XP_016878671.1:p.Glu800AsnfsTer?
XM_017023183.1:c.2398_2401del XP_016878672.1:p.Glu800AsnfsTer?
XM_017023184.1:c.2398_2401del XP_016878673.1:p.Glu800AsnfsTer?
XM_017023185.1:c.2398_2401del XP_016878674.1:p.Glu800AsnfsTer?
XM_017023186.1:c.2398_2401del XP_016878675.1:p.Glu800AsnfsTer?
XM_017023187.1:c.2398_2401del XP_016878676.1:p.Glu800AsnfsTer?
XM_024450244.1:c.2296_2299del XP_024306012.1:p.Glu766AsnfsTer?
NM_013275.6:c.2398_2401del MANE Select NP_037407.4:p.Glu800AsnfsTer?
NM_001256182.2:c.2398_2401del NP_001243111.1:p.Glu800AsnfsTer?
NM_001256183.2:c.2398_2401del NP_001243112.1:p.Glu800AsnfsTer?