Canonical Allele Identifier: CA208327541
Gene: ANK3 HGNC NCBI

Linked Data

dbSNP Id: rs4948418

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60425736C>T , CM000672.2:g.60425736C>T GRCh38
NC_000010.10:g.62185494C>T , CM000672.1:g.62185494C>T GRCh37
NC_000010.9:g.61855500C>T NCBI36
NG_029917.1:g.312791G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000503366.6:c.64-146097G>A ENSP00000425236.1:n.64-146097G>A
ENST00000373827.6:c.97-146097G>A ENSP00000362933.2:n.97-146097G>A
ENST00000503366.5:c.64-146097G>A ENSP00000425236.1:n.64-146097G>A
ENST00000622427.4:c.64-146097G>A ENSP00000483244.1:n.64-146097G>A
NM_001204403.1:c.97-146097G>A NP_001191332.1:n.97-146097G>A
NM_001204404.1:c.64-146097G>A NP_001191333.1:n.64-146097G>A
XM_011539700.1:c.103-146097G>A XP_011538002.1:n.103-146097G>A
XM_011539701.1:c.97-146097G>A XP_011538003.1:n.97-146097G>A
XM_011539702.1:c.58-146097G>A XP_011538004.1:n.58-146097G>A
XM_011539704.1:c.15+72248G>A XP_011538006.1:n.15+72248G>A
XM_017016114.1:c.64-146097G>A XP_016871603.1:n.64-146097G>A
XM_024447958.1:c.64-146097G>A XP_024303726.1:n.64-146097G>A
NM_001204403.2:c.97-146097G>A NP_001191332.1:n.97-146097G>A
NM_001204404.2:c.64-146097G>A NP_001191333.1:n.64-146097G>A