Canonical Allele Identifier: CA10603565
Gene: ANKRD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89283812_89283823delinsA , CM000678.2:g.89283812_89283823delinsA GRCh38
NC_000016.9:g.89350220_89350231delinsA , CM000678.1:g.89350220_89350231delinsA GRCh37
NC_000016.8:g.87877721_87877732delinsA NCBI36
NG_032003.1:g.211739_211750delinsT
NG_032003.2:g.211739_211750delinsT

Transcript Alleles

HGVS Amino-acid Change
ENST00000301030.10:c.2719_2730delinsT MANE Select ENSP00000301030.4:p.Lys907Ter
ENST00000330736.10:c.*2522_*2533delinsT ENSP00000330815.5:n.*2522_*2533delinsT
ENST00000378330.7:c.2719_2730delinsT ENSP00000367581.2:p.Lys907Ter
ENST00000642443.1:c.2344_2355delinsT ENSP00000493644.1:p.Lys782Ter
ENST00000642600.1:c.2719_2730delinsT ENSP00000495226.1:p.Lys907Ter
ENST00000644285.1:c.744+4705_744+4716delinsT ENSP00000496476.1:n.744+4705_744+4716delinsT
ENST00000301030.8:c.2719_2730delinsT ENSP00000301030.4:p.Lys907Ter
ENST00000330736.9:c.*2522_*2533delinsT ENSP00000330815.5:n.*2522_*2533delinsT
ENST00000378330.6:c.2719_2730delinsT ENSP00000367581.2:p.Lys907Ter
ENST00000562194.1:c.151+4705_151+4716delinsT
NM_001256182.1:c.2719_2730delinsT NP_001243111.1:p.Lys907Ter
NM_001256183.1:c.2719_2730delinsT NP_001243112.1:p.Lys907Ter
NM_013275.5:c.2719_2730delinsT NP_037407.4:p.Lys907Ter
XM_006721181.1:c.2617_2628delinsT XP_006721244.1:p.Lys873Ter
XM_006721184.2:c.2422_2433delinsT XP_006721247.1:p.Lys808Ter
XM_011523051.1:c.2719_2730delinsT XP_011521353.1:p.Lys907Ter
XM_011523052.1:c.2719_2730delinsT XP_011521354.1:p.Lys907Ter
XM_011523053.1:c.2719_2730delinsT XP_011521355.1:p.Lys907Ter
XM_011523054.1:c.2617_2628delinsT XP_011521356.1:p.Lys873Ter
XM_011523055.1:c.2617_2628delinsT XP_011521357.1:p.Lys873Ter
XM_011523056.1:c.2590_2601delinsT XP_011521358.1:p.Lys864Ter
XM_011523057.1:c.2719_2730delinsT XP_011521359.1:p.Lys907Ter
XM_011523051.3:c.2719_2730delinsT XP_011521353.1:p.Lys907Ter
XM_011523053.2:c.2719_2730delinsT XP_011521355.1:p.Lys907Ter
XM_011523054.2:c.2617_2628delinsT XP_011521356.1:p.Lys873Ter
XM_011523055.2:c.2617_2628delinsT XP_011521357.1:p.Lys873Ter
XM_011523056.2:c.2590_2601delinsT XP_011521358.1:p.Lys864Ter
XM_011523057.2:c.2719_2730delinsT XP_011521359.1:p.Lys907Ter
XM_017023182.2:c.2719_2730delinsT XP_016878671.1:p.Lys907Ter
XM_017023183.1:c.2719_2730delinsT XP_016878672.1:p.Lys907Ter
XM_017023184.1:c.2719_2730delinsT XP_016878673.1:p.Lys907Ter
XM_017023185.1:c.2719_2730delinsT XP_016878674.1:p.Lys907Ter
XM_017023186.1:c.2719_2730delinsT XP_016878675.1:p.Lys907Ter
XM_017023187.1:c.2719_2730delinsT XP_016878676.1:p.Lys907Ter
XM_024450244.1:c.2617_2628delinsT XP_024306012.1:p.Lys873Ter
NM_013275.6:c.2719_2730delinsT MANE Select NP_037407.4:p.Lys907Ter
NM_001256182.2:c.2719_2730delinsT NP_001243111.1:p.Lys907Ter
NM_001256183.2:c.2719_2730delinsT NP_001243112.1:p.Lys907Ter