Canonical Allele Identifier: CA645294091
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 426290
ClinVar RCV Id: RCV000489674
dbSNP Id: rs1085307544
MyVariant Identifiers: chr16:g.89348745dup (hg19) chr16:g.89348744_89348745insT (hg19) chr16:g.89282337dup (hg38) chr16:g.89282336_89282337insT (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89282337dup , CM000678.2:g.89282337dup GRCh38
NC_000016.9:g.89348745dup , CM000678.1:g.89348745dup GRCh37
NC_000016.8:g.87876246dup NCBI36
NG_032003.1:g.213225dup
NG_032003.2:g.213225dup

Transcript Alleles

HGVS Amino-acid change
ENST00000301030.10:c.4205dup MANE Select ENSP00000301030.4:p.Tyr1402Ter
ENST00000330736.10:c.*4008dup ENSP00000330815.5:n.*4008dup
ENST00000378330.7:c.4205dup ENSP00000367581.2:p.Tyr1402Ter
ENST00000642600.1:c.4205dup ENSP00000495226.1:p.Tyr1402Ter
ENST00000644285.1:c.744+6191dup ENSP00000496476.1:n.744+6191dup
ENST00000301030.8:c.4205dup ENSP00000301030.4:p.Tyr1402Ter
ENST00000330736.9:c.*4008dup ENSP00000330815.5:n.*4008dup
ENST00000378330.6:c.4205dup ENSP00000367581.2:p.Tyr1402Ter
ENST00000562194.1:c.151+6191dup
NM_001256182.1:c.4205dup NP_001243111.1:p.Tyr1402Ter
NM_001256183.1:c.4205dup NP_001243112.1:p.Tyr1402Ter
NM_013275.5:c.4205dup NP_037407.4:p.Tyr1402Ter
XM_006721181.1:c.4103dup XP_006721244.1:p.Tyr1368Ter
XM_006721184.2:c.3908dup XP_006721247.1:p.Tyr1303Ter
XM_011523051.1:c.4205dup XP_011521353.1:p.Tyr1402Ter
XM_011523052.1:c.4205dup XP_011521354.1:p.Tyr1402Ter
XM_011523053.1:c.4205dup XP_011521355.1:p.Tyr1402Ter
XM_011523054.1:c.4103dup XP_011521356.1:p.Tyr1368Ter
XM_011523055.1:c.4103dup XP_011521357.1:p.Tyr1368Ter
XM_011523056.1:c.4076dup XP_011521358.1:p.Tyr1359Ter
XM_011523057.1:c.4205dup XP_011521359.1:p.Tyr1402Ter
XM_011523051.3:c.4205dup XP_011521353.1:p.Tyr1402Ter
XM_011523053.2:c.4205dup XP_011521355.1:p.Tyr1402Ter
XM_011523054.2:c.4103dup XP_011521356.1:p.Tyr1368Ter
XM_011523055.2:c.4103dup XP_011521357.1:p.Tyr1368Ter
XM_011523056.2:c.4076dup XP_011521358.1:p.Tyr1359Ter
XM_011523057.2:c.4205dup XP_011521359.1:p.Tyr1402Ter
XM_017023182.2:c.4205dup XP_016878671.1:p.Tyr1402Ter
XM_017023183.1:c.4205dup XP_016878672.1:p.Tyr1402Ter
XM_017023184.1:c.4205dup XP_016878673.1:p.Tyr1402Ter
XM_017023185.1:c.4205dup XP_016878674.1:p.Tyr1402Ter
XM_017023186.1:c.4205dup XP_016878675.1:p.Tyr1402Ter
XM_017023187.1:c.4205dup XP_016878676.1:p.Tyr1402Ter
XM_024450244.1:c.4103dup XP_024306012.1:p.Tyr1368Ter
NM_013275.6:c.4205dup MANE Select NP_037407.4:p.Tyr1402Ter
NM_001256182.2:c.4205dup NP_001243111.1:p.Tyr1402Ter
NM_001256183.2:c.4205dup NP_001243112.1:p.Tyr1402Ter
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