Canonical Allele Identifier: CA204700
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 208695
ClinVar RCV Id: RCV000190712 RCV000335440 RCV001265123
dbSNP Id: rs797044890
MyVariant Identifiers: chr16:g.89341500C>T (hg19) chr16:g.89275092C>T (hg38)
PubMed: PMID:25356970
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89275092C>T , CM000678.2:g.89275092C>T GRCh38
NC_000016.9:g.89341500C>T , CM000678.1:g.89341500C>T GRCh37
NC_000016.8:g.87869001C>T NCBI36
NG_032003.1:g.220470G>A
NG_032003.2:g.220470G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000301030.10:c.7569+1G>A MANE Select ENSP00000301030.4:n.7569+1G>A
ENST00000330736.10:c.*7372+1G>A ENSP00000330815.5:n.*7372+1G>A
ENST00000378330.7:c.7569+1G>A ENSP00000367581.2:n.7569+1G>A
ENST00000642600.1:c.7569+1G>A ENSP00000495226.1:n.7569+1G>A
ENST00000644285.1:c.843+1G>A ENSP00000496476.1:n.843+1G>A
ENST00000645666.1:n.26+1G>A
ENST00000301030.8:c.7569+1G>A ENSP00000301030.4:n.7569+1G>A
ENST00000330736.9:c.*7372+1G>A ENSP00000330815.5:n.*7372+1G>A
ENST00000378330.6:c.7569+1G>A ENSP00000367581.2:n.7569+1G>A
ENST00000562194.1:c.250+1G>A
NM_001256182.1:c.7569+1G>A NP_001243111.1:n.7569+1G>A
NM_001256183.1:c.7569+1G>A NP_001243112.1:n.7569+1G>A
NM_013275.5:c.7569+1G>A NP_037407.4:n.7569+1G>A
XM_006721181.1:c.7467+1G>A XP_006721244.1:n.7467+1G>A
XM_006721184.2:c.7272+1G>A XP_006721247.1:n.7272+1G>A
XM_011523051.1:c.7569+1G>A XP_011521353.1:n.7569+1G>A
XM_011523052.1:c.7569+1G>A XP_011521354.1:n.7569+1G>A
XM_011523053.1:c.7569+1G>A XP_011521355.1:n.7569+1G>A
XM_011523054.1:c.7467+1G>A XP_011521356.1:n.7467+1G>A
XM_011523055.1:c.7467+1G>A XP_011521357.1:n.7467+1G>A
XM_011523056.1:c.7440+1G>A XP_011521358.1:n.7440+1G>A
XM_011523057.1:c.7569+1G>A XP_011521359.1:n.7569+1G>A
XM_011523051.3:c.7569+1G>A XP_011521353.1:n.7569+1G>A
XM_011523053.2:c.7569+1G>A XP_011521355.1:n.7569+1G>A
XM_011523054.2:c.7467+1G>A XP_011521356.1:n.7467+1G>A
XM_011523055.2:c.7467+1G>A XP_011521357.1:n.7467+1G>A
XM_011523056.2:c.7440+1G>A XP_011521358.1:n.7440+1G>A
XM_011523057.2:c.7569+1G>A XP_011521359.1:n.7569+1G>A
XM_017023182.2:c.7569+1G>A XP_016878671.1:n.7569+1G>A
XM_017023183.1:c.7569+1G>A XP_016878672.1:n.7569+1G>A
XM_017023184.1:c.7569+1G>A XP_016878673.1:n.7569+1G>A
XM_017023185.1:c.7569+1G>A XP_016878674.1:n.7569+1G>A
XM_017023186.1:c.7569+1G>A XP_016878675.1:n.7569+1G>A
XM_017023187.1:c.7569+1G>A XP_016878676.1:n.7569+1G>A
XM_024450244.1:c.7467+1G>A XP_024306012.1:n.7467+1G>A
NM_013275.6:c.7569+1G>A MANE Select NP_037407.4:n.7569+1G>A
NM_001256182.2:c.7569+1G>A NP_001243111.1:n.7569+1G>A
NM_001256183.2:c.7569+1G>A NP_001243112.1:n.7569+1G>A
Search 100 bp 5'
Search 100 bp 3'