Canonical Allele Identifier: CA2588773823
Gene: ANK3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60462440T>C , CM000672.2:g.60462440T>C GRCh38
NC_000010.10:g.62222198T>C , CM000672.1:g.62222198T>C GRCh37
NC_000010.9:g.61892204T>C NCBI36
NG_029917.1:g.276087A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000503366.6:c.63+110025A>G ENSP00000425236.1:n.63+110025A>G
ENST00000373827.6:c.96+152746A>G ENSP00000362933.2:n.96+152746A>G
ENST00000503366.5:c.63+110025A>G ENSP00000425236.1:n.63+110025A>G
ENST00000622427.4:c.63+110025A>G ENSP00000483244.1:n.63+110025A>G
NM_001204403.1:c.96+152746A>G NP_001191332.1:n.96+152746A>G
NM_001204404.1:c.63+110025A>G NP_001191333.1:n.63+110025A>G
XM_011539700.1:c.102+152746A>G XP_011538002.1:n.102+152746A>G
XM_011539701.1:c.96+152746A>G XP_011538003.1:n.96+152746A>G
XM_011539702.1:c.58-182801A>G XP_011538004.1:n.58-182801A>G
XM_011539704.1:c.15+35544A>G XP_011538006.1:n.15+35544A>G
XM_017016114.1:c.63+110025A>G XP_016871603.1:n.63+110025A>G
XM_024447958.1:c.63+110025A>G XP_024303726.1:n.63+110025A>G
NM_001204403.2:c.96+152746A>G NP_001191332.1:n.96+152746A>G
NM_001204404.2:c.63+110025A>G NP_001191333.1:n.63+110025A>G