Canonical Allele Identifier: CA2788194340
Gene: ANK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60425637del , CM000672.2:g.60425637del GRCh38
NC_000010.10:g.62185395del , CM000672.1:g.62185395del GRCh37
NC_000010.9:g.61855401del NCBI36
NG_029917.1:g.312890del

Transcript Alleles

HGVS Amino-acid change
ENST00000503366.6:c.64-145998del ENSP00000425236.1:n.64-145998del
ENST00000373827.6:c.97-145998del ENSP00000362933.2:n.97-145998del
ENST00000503366.5:c.64-145998del ENSP00000425236.1:n.64-145998del
ENST00000622427.4:c.64-145998del ENSP00000483244.1:n.64-145998del
NM_001204403.1:c.97-145998del NP_001191332.1:n.97-145998del
NM_001204404.1:c.64-145998del NP_001191333.1:n.64-145998del
XM_011539700.1:c.103-145998del XP_011538002.1:n.103-145998del
XM_011539701.1:c.97-145998del XP_011538003.1:n.97-145998del
XM_011539702.1:c.58-145998del XP_011538004.1:n.58-145998del
XM_011539704.1:c.15+72347del XP_011538006.1:n.15+72347del
XM_017016114.1:c.64-145998del XP_016871603.1:n.64-145998del
XM_024447958.1:c.64-145998del XP_024303726.1:n.64-145998del
NM_001204403.2:c.97-145998del NP_001191332.1:n.97-145998del
NM_001204404.2:c.64-145998del NP_001191333.1:n.64-145998del