Canonical Allele Identifier: CA397167304

Gene: ANKRD11

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89290721C>A , CM000678.2:g.89290721C>A	GRCh38
NC_000016.9:g.89357129C>A , CM000678.1:g.89357129C>A	GRCh37
NC_000016.8:g.87884630C>A	NCBI36
NG_032003.1:g.204841G>T
NG_032003.2:g.204841G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_013275.6:c.505G>T MANE Select	NP_037407.4:p.Glu169Ter
ENST00000301030.10:c.505G>T MANE Select	ENSP00000301030.4:p.Glu169Ter
NM_001256182.1:c.505G>T	NP_001243111.1:p.Glu169Ter
NM_001256182.2:c.505G>T	NP_001243111.1:p.Glu169Ter
NM_001256183.1:c.505G>T	NP_001243112.1:p.Glu169Ter
NM_001256183.2:c.505G>T	NP_001243112.1:p.Glu169Ter
NM_013275.5:c.505G>T	NP_037407.4:p.Glu169Ter
NR_045839.1:n.1336G>T
NR_045839.2:n.1336G>T
ENST00000301030.8:c.505G>T	ENSP00000301030.4:p.Glu169Ter
ENST00000330736.10:c.*308G>T	ENSP00000330815.5:n.*308G>T
ENST00000330736.9:c.*308G>T	ENSP00000330815.5:n.*308G>T
ENST00000378330.6:c.505G>T	ENSP00000367581.2:p.Glu169Ter
ENST00000378330.7:c.505G>T	ENSP00000367581.2:p.Glu169Ter
ENST00000378332.6:c.*767G>T	ENSP00000367583.2:n.*767G>T
ENST00000378332.7:c.*767G>T	ENSP00000367583.2:n.*767G>T
ENST00000562275.5:c.*308G>T	ENSP00000454550.1:n.*308G>T
ENST00000562275.6:c.*308G>T	ENSP00000454550.1:n.*308G>T
ENST00000567699.2:n.444-4535G>T
ENST00000613312.4:c.505G>T	ENSP00000478018.1:p.Glu169Ter
ENST00000642333.1:c.505G>T	ENSP00000496651.1:p.Glu169Ter
ENST00000642443.1:c.227-2051G>T	ENSP00000493644.1:n.227-2051G>T
ENST00000642600.1:c.505G>T	ENSP00000495226.1:p.Glu169Ter
ENST00000642695.1:c.505G>T	ENSP00000495449.1:p.Glu169Ter
ENST00000643964.1:c.*308G>T	ENSP00000495181.1:n.*308G>T
ENST00000644285.1:c.505G>T	ENSP00000496476.1:p.Glu169Ter
ENST00000644784.1:c.505G>T	ENSP00000496419.1:p.Glu169Ter
ENST00000645278.1:c.*135G>T	ENSP00000494850.1:n.*135G>T
ENST00000646345.1:n.497G>T
ENST00000646838.1:c.505G>T	ENSP00000495124.1:p.Glu169Ter
ENST00000646975.1:c.505G>T	ENSP00000495608.1:p.Glu169Ter
XM_006721181.1:c.403G>T	XP_006721244.1:p.Glu135Ter
XM_006721184.2:c.208G>T	XP_006721247.1:p.Glu70Ter
XM_011523051.1:c.505G>T	XP_011521353.1:p.Glu169Ter
XM_011523051.3:c.505G>T	XP_011521353.1:p.Glu169Ter
XM_011523052.1:c.505G>T	XP_011521354.1:p.Glu169Ter
XM_011523053.1:c.505G>T	XP_011521355.1:p.Glu169Ter
XM_011523053.2:c.505G>T	XP_011521355.1:p.Glu169Ter
XM_011523054.1:c.403G>T	XP_011521356.1:p.Glu135Ter
XM_011523054.2:c.403G>T	XP_011521356.1:p.Glu135Ter
XM_011523055.1:c.403G>T	XP_011521357.1:p.Glu135Ter
XM_011523055.2:c.403G>T	XP_011521357.1:p.Glu135Ter
XM_011523056.1:c.376G>T	XP_011521358.1:p.Glu126Ter
XM_011523056.2:c.376G>T	XP_011521358.1:p.Glu126Ter
XM_011523057.1:c.505G>T	XP_011521359.1:p.Glu169Ter
XM_011523057.2:c.505G>T	XP_011521359.1:p.Glu169Ter
XM_017023182.2:c.505G>T	XP_016878671.1:p.Glu169Ter
XM_017023183.1:c.505G>T	XP_016878672.1:p.Glu169Ter
XM_017023184.1:c.505G>T	XP_016878673.1:p.Glu169Ter
XM_017023185.1:c.505G>T	XP_016878674.1:p.Glu169Ter
XM_017023186.1:c.505G>T	XP_016878675.1:p.Glu169Ter
XM_017023187.1:c.505G>T	XP_016878676.1:p.Glu169Ter
XM_024450244.1:c.403G>T	XP_024306012.1:p.Glu135Ter