Canonical Allele Identifier: CA10603283
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 280842
ClinVar RCV Id: RCV000361760
dbSNP Id: rs886041976

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89270911T>C , CM000678.2:g.89270911T>C GRCh38
NC_000016.9:g.89337319T>C , CM000678.1:g.89337319T>C GRCh37
NC_000016.8:g.87864820T>C NCBI36
NG_032003.1:g.224651A>G
NG_032003.2:g.224651A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000301030.10:c.7714-2A>G MANE Select ENSP00000301030.4:p.=
ENST00000330736.10:c.*7517-2A>G ENSP00000330815.5:p.=
ENST00000378330.7:c.7714-2A>G ENSP00000367581.2:p.=
ENST00000642600.1:c.7714-2A>G ENSP00000495226.1:p.=
ENST00000644285.1:n.988-2A>G ENSP00000496476.1:p.=
ENST00000301030.8:c.7714-2A>G ENSP00000301030.4:p.=
ENST00000330736.9:c.*7517-2A>G ENSP00000330815.5:p.=
ENST00000378330.6:c.7714-2A>G ENSP00000367581.2:p.=
ENST00000562194.1:n.395-2A>G
NM_001256182.1:c.7714-2A>G NP_001243111.1:p.=
NM_001256183.1:c.7714-2A>G NP_001243112.1:p.=
NM_013275.5:c.7714-2A>G NP_037407.4:p.=
XM_006721181.1:c.7612-2A>G XP_006721244.1:p.=
XM_006721184.2:c.7417-2A>G XP_006721247.1:p.=
XM_011523051.1:c.7714-2A>G XP_011521353.1:p.=
XM_011523052.1:c.7714-2A>G XP_011521354.1:p.=
XM_011523053.1:c.7714-2A>G XP_011521355.1:p.=
XM_011523054.1:c.7612-2A>G XP_011521356.1:p.=
XM_011523055.1:c.7612-2A>G XP_011521357.1:p.=
XM_011523056.1:c.7585-2A>G XP_011521358.1:p.=
XM_011523057.1:c.7714-2A>G XP_011521359.1:p.=
XM_011523051.3:c.7714-2A>G XP_011521353.1:p.=
XM_011523053.2:c.7714-2A>G XP_011521355.1:p.=
XM_011523054.2:c.7612-2A>G XP_011521356.1:p.=
XM_011523055.2:c.7612-2A>G XP_011521357.1:p.=
XM_011523056.2:c.7585-2A>G XP_011521358.1:p.=
XM_011523057.2:c.7714-2A>G XP_011521359.1:p.=
XM_017023182.2:c.7714-2A>G XP_016878671.1:p.=
XM_017023183.1:c.7714-2A>G XP_016878672.1:p.=
XM_017023184.1:c.7714-2A>G XP_016878673.1:p.=
XM_017023185.1:c.7714-2A>G XP_016878674.1:p.=
XM_017023186.1:c.7714-2A>G XP_016878675.1:p.=
XM_017023187.1:c.7714-2A>G XP_016878676.1:p.=
XM_024450244.1:c.7612-2A>G XP_024306012.1:p.=
NM_013275.6:c.7714-2A>G MANE Select NP_037407.4:p.=
NM_001256182.2:c.7714-2A>G NP_001243111.1:p.=
NM_001256183.2:c.7714-2A>G NP_001243112.1:p.=