Canonical Allele Identifier: CA10603284
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 280655
ClinVar RCV Id: RCV000324877
dbSNP Id: rs886041822
MyVariant Identifiers: chr16:g.89345867dupG (hg19) chr16:g.89345866_89345867insG (hg19) chr16:g.89279459dupG (hg38) chr16:g.89279458_89279459insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89279463dup , CM000678.2:g.89279463dup GRCh38
NC_000016.9:g.89345871dup , CM000678.1:g.89345871dup GRCh37
NC_000016.8:g.87873372dup NCBI36
NG_032003.1:g.216103dup
NG_032003.2:g.216103dup

Transcript Alleles

HGVS Amino-acid change
ENST00000301030.10:c.7083dup MANE Select ENSP00000301030.4:p.Thr2362HisfsTer?
ENST00000330736.10:c.*6886dup ENSP00000330815.5:n.*6886dup
ENST00000378330.7:c.7083dup ENSP00000367581.2:p.Thr2362HisfsTer?
ENST00000642600.1:c.7083dup ENSP00000495226.1:p.Thr2362HisfsTer?
ENST00000644285.1:c.745-4268dup ENSP00000496476.1:n.745-4268dup
ENST00000301030.8:c.7083dup ENSP00000301030.4:p.Thr2362HisfsTer?
ENST00000330736.9:c.*6886dup ENSP00000330815.5:n.*6886dup
ENST00000378330.6:c.7083dup ENSP00000367581.2:p.Thr2362HisfsTer?
ENST00000562194.1:c.152-4268dup
ENST00000623388.1:n.258dup
NM_001256182.1:c.7083dup NP_001243111.1:p.Thr2362HisfsTer?
NM_001256183.1:c.7083dup NP_001243112.1:p.Thr2362HisfsTer?
NM_013275.5:c.7083dup NP_037407.4:p.Thr2362HisfsTer?
XM_006721181.1:c.6981dup XP_006721244.1:p.Thr2328HisfsTer?
XM_006721184.2:c.6786dup XP_006721247.1:p.Thr2263HisfsTer?
XM_011523051.1:c.7083dup XP_011521353.1:p.Thr2362HisfsTer?
XM_011523052.1:c.7083dup XP_011521354.1:p.Thr2362HisfsTer?
XM_011523053.1:c.7083dup XP_011521355.1:p.Thr2362HisfsTer?
XM_011523054.1:c.6981dup XP_011521356.1:p.Thr2328HisfsTer?
XM_011523055.1:c.6981dup XP_011521357.1:p.Thr2328HisfsTer?
XM_011523056.1:c.6954dup XP_011521358.1:p.Thr2319HisfsTer?
XM_011523057.1:c.7083dup XP_011521359.1:p.Thr2362HisfsTer?
XM_011523051.3:c.7083dup XP_011521353.1:p.Thr2362HisfsTer?
XM_011523053.2:c.7083dup XP_011521355.1:p.Thr2362HisfsTer?
XM_011523054.2:c.6981dup XP_011521356.1:p.Thr2328HisfsTer?
XM_011523055.2:c.6981dup XP_011521357.1:p.Thr2328HisfsTer?
XM_011523056.2:c.6954dup XP_011521358.1:p.Thr2319HisfsTer?
XM_011523057.2:c.7083dup XP_011521359.1:p.Thr2362HisfsTer?
XM_017023182.2:c.7083dup XP_016878671.1:p.Thr2362HisfsTer?
XM_017023183.1:c.7083dup XP_016878672.1:p.Thr2362HisfsTer?
XM_017023184.1:c.7083dup XP_016878673.1:p.Thr2362HisfsTer?
XM_017023185.1:c.7083dup XP_016878674.1:p.Thr2362HisfsTer?
XM_017023186.1:c.7083dup XP_016878675.1:p.Thr2362HisfsTer?
XM_017023187.1:c.7083dup XP_016878676.1:p.Thr2362HisfsTer?
XM_024450244.1:c.6981dup XP_024306012.1:p.Thr2328HisfsTer?
NM_013275.6:c.7083dup MANE Select NP_037407.4:p.Thr2362HisfsTer?
NM_001256182.2:c.7083dup NP_001243111.1:p.Thr2362HisfsTer?
NM_001256183.2:c.7083dup NP_001243112.1:p.Thr2362HisfsTer?
Search 100 bp 5'
Search 100 bp 3'