Canonical Allele Identifier: CA928994034
Gene: ANK3 HGNC NCBI

Linked Data

dbSNP Id: rs2064903895

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60462244_60462246del , CM000672.2:g.60462244_60462246del GRCh38
NC_000010.10:g.62222002_62222004del , CM000672.1:g.62222002_62222004del GRCh37
NC_000010.9:g.61892008_61892010del NCBI36
NG_029917.1:g.276283_276285del

Transcript Alleles

HGVS Amino-acid Change
ENST00000503366.6:c.63+110221_63+110223del ENSP00000425236.1:n.63+110221_63+110223del
ENST00000373827.6:c.96+152942_96+152944del ENSP00000362933.2:n.96+152942_96+152944del
ENST00000503366.5:c.63+110221_63+110223del ENSP00000425236.1:n.63+110221_63+110223del
ENST00000622427.4:c.63+110221_63+110223del ENSP00000483244.1:n.63+110221_63+110223del
NM_001204403.1:c.96+152942_96+152944del NP_001191332.1:n.96+152942_96+152944del
NM_001204404.1:c.63+110221_63+110223del NP_001191333.1:n.63+110221_63+110223del
XM_011539700.1:c.102+152942_102+152944del XP_011538002.1:n.102+152942_102+152944del
XM_011539701.1:c.96+152942_96+152944del XP_011538003.1:n.96+152942_96+152944del
XM_011539702.1:c.58-182605_58-182603del XP_011538004.1:n.58-182605_58-182603del
XM_011539704.1:c.15+35740_15+35742del XP_011538006.1:n.15+35740_15+35742del
XM_017016114.1:c.63+110221_63+110223del XP_016871603.1:n.63+110221_63+110223del
XM_024447958.1:c.63+110221_63+110223del XP_024303726.1:n.63+110221_63+110223del
NM_001204403.2:c.96+152942_96+152944del NP_001191332.1:n.96+152942_96+152944del
NM_001204404.2:c.63+110221_63+110223del NP_001191333.1:n.63+110221_63+110223del