Canonical Allele Identifier: CA2241603339
Gene: ANKRD11 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89282629A= , CM000678.2:g.89282629A= GRCh38
NC_000016.9:g.89349037A= , CM000678.1:g.89349037A= GRCh37
NC_000016.8:g.87876538A= NCBI36
NG_032003.1:g.212933T=
NG_032003.2:g.212933T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000301030.10:c.3913T= MANE Select ENSP00000301030.4:p.Ser1305=
ENST00000330736.10:c.*3716T= ENSP00000330815.5:n.*3716T=
ENST00000378330.7:c.3913T= ENSP00000367581.2:p.Ser1305=
ENST00000642600.1:c.3913T= ENSP00000495226.1:p.Ser1305=
ENST00000644285.1:c.744+5899T= ENSP00000496476.1:n.744+5899T=
ENST00000301030.8:c.3913T= ENSP00000301030.4:p.Ser1305=
ENST00000330736.9:c.*3716T= ENSP00000330815.5:n.*3716T=
ENST00000378330.6:c.3913T= ENSP00000367581.2:p.Ser1305=
ENST00000562194.1:c.151+5899T=
NM_001256182.1:c.3913T= NP_001243111.1:p.Ser1305=
NM_001256183.1:c.3913T= NP_001243112.1:p.Ser1305=
NM_013275.5:c.3913T= NP_037407.4:p.Ser1305=
XM_006721181.1:c.3811T= XP_006721244.1:p.Ser1271=
XM_006721184.2:c.3616T= XP_006721247.1:p.Ser1206=
XM_011523051.1:c.3913T= XP_011521353.1:p.Ser1305=
XM_011523052.1:c.3913T= XP_011521354.1:p.Ser1305=
XM_011523053.1:c.3913T= XP_011521355.1:p.Ser1305=
XM_011523054.1:c.3811T= XP_011521356.1:p.Ser1271=
XM_011523055.1:c.3811T= XP_011521357.1:p.Ser1271=
XM_011523056.1:c.3784T= XP_011521358.1:p.Ser1262=
XM_011523057.1:c.3913T= XP_011521359.1:p.Ser1305=
XM_011523051.3:c.3913T= XP_011521353.1:p.Ser1305=
XM_011523053.2:c.3913T= XP_011521355.1:p.Ser1305=
XM_011523054.2:c.3811T= XP_011521356.1:p.Ser1271=
XM_011523055.2:c.3811T= XP_011521357.1:p.Ser1271=
XM_011523056.2:c.3784T= XP_011521358.1:p.Ser1262=
XM_011523057.2:c.3913T= XP_011521359.1:p.Ser1305=
XM_017023182.2:c.3913T= XP_016878671.1:p.Ser1305=
XM_017023183.1:c.3913T= XP_016878672.1:p.Ser1305=
XM_017023184.1:c.3913T= XP_016878673.1:p.Ser1305=
XM_017023185.1:c.3913T= XP_016878674.1:p.Ser1305=
XM_017023186.1:c.3913T= XP_016878675.1:p.Ser1305=
XM_017023187.1:c.3913T= XP_016878676.1:p.Ser1305=
XM_024450244.1:c.3811T= XP_024306012.1:p.Ser1271=
NM_013275.6:c.3913T= MANE Select NP_037407.4:p.Ser1305=
NM_001256182.2:c.3913T= NP_001243111.1:p.Ser1305=
NM_001256183.2:c.3913T= NP_001243112.1:p.Ser1305=