Canonical Allele Identifier: CA2580598560
Gene: ANK3 HGNC NCBI

Linked Data

dbSNP Id: rs10994397

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60519366C>A , CM000672.2:g.60519366C>A GRCh38
NC_000010.10:g.62279124C>A , CM000672.1:g.62279124C>A GRCh37
NC_000010.9:g.61949130C>A NCBI36
NG_029917.1:g.219161G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000503366.6:c.63+53099G>T ENSP00000425236.1:n.63+53099G>T
ENST00000373827.6:c.96+95820G>T ENSP00000362933.2:n.96+95820G>T
ENST00000503366.5:c.63+53099G>T ENSP00000425236.1:n.63+53099G>T
ENST00000510382.1:n.102-10741G>T
ENST00000622427.4:c.63+53099G>T ENSP00000483244.1:n.63+53099G>T
NM_001204403.1:c.96+95820G>T NP_001191332.1:n.96+95820G>T
NM_001204404.1:c.63+53099G>T NP_001191333.1:n.63+53099G>T
XM_011539700.1:c.102+95820G>T XP_011538002.1:n.102+95820G>T
XM_011539701.1:c.96+95820G>T XP_011538003.1:n.96+95820G>T
XM_011539702.1:c.57+213897G>T XP_011538004.1:n.57+213897G>T
XM_017016114.1:c.63+53099G>T XP_016871603.1:n.63+53099G>T
XM_024447958.1:c.63+53099G>T XP_024303726.1:n.63+53099G>T
NM_001204403.2:c.96+95820G>T NP_001191332.1:n.96+95820G>T
NM_001204404.2:c.63+53099G>T NP_001191333.1:n.63+53099G>T