Canonical Allele Identifier: CA667039333
Gene: ANK3 HGNC NCBI

Linked Data

dbSNP Id: rs1412011955

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60421382_60421386del , CM000672.2:g.60421382_60421386del GRCh38
NC_000010.10:g.62181140_62181144del , CM000672.1:g.62181140_62181144del GRCh37
NC_000010.9:g.61851146_61851150del NCBI36
NG_029917.1:g.317142_317146del

Transcript Alleles

HGVS Amino-acid change
ENST00000503366.6:c.64-141746_64-141742del ENSP00000425236.1:n.64-141746_64-141742de...
ENST00000373827.6:c.97-141746_97-141742del ENSP00000362933.2:n.97-141746_97-141742de...
ENST00000503366.5:c.64-141746_64-141742del ENSP00000425236.1:n.64-141746_64-141742de...
ENST00000622427.4:c.64-141746_64-141742del ENSP00000483244.1:n.64-141746_64-141742de...
NM_001204403.1:c.97-141746_97-141742del NP_001191332.1:n.97-141746_97-141742del
NM_001204404.1:c.64-141746_64-141742del NP_001191333.1:n.64-141746_64-141742del
XM_011539700.1:c.103-141746_103-141742del XP_011538002.1:n.103-141746_103-141742del...
XM_011539701.1:c.97-141746_97-141742del XP_011538003.1:n.97-141746_97-141742del
XM_011539702.1:c.58-141746_58-141742del XP_011538004.1:n.58-141746_58-141742del
XM_011539704.1:c.15+76599_15+76603del XP_011538006.1:n.15+76599_15+76603del
XM_017016114.1:c.64-141746_64-141742del XP_016871603.1:n.64-141746_64-141742del
XM_024447958.1:c.64-141746_64-141742del XP_024303726.1:n.64-141746_64-141742del
NM_001204403.2:c.97-141746_97-141742del NP_001191332.1:n.97-141746_97-141742del
NM_001204404.2:c.64-141746_64-141742del NP_001191333.1:n.64-141746_64-141742del