Canonical Allele Identifier: CA2721602091

Gene: ANK3

Linked Data

• dbSNP Id: rs1595193519

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60519349C>T , CM000672.2:g.60519349C>T	GRCh38
NC_000010.10:g.62279107C>T , CM000672.1:g.62279107C>T	GRCh37
NC_000010.9:g.61949113C>T	NCBI36
NG_029917.1:g.219178G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000503366.6:c.63+53116G>A	ENSP00000425236.1:n.63+53116G>A
ENST00000373827.6:c.96+95837G>A	ENSP00000362933.2:n.96+95837G>A
ENST00000503366.5:c.63+53116G>A	ENSP00000425236.1:n.63+53116G>A
ENST00000510382.1:n.102-10724G>A
ENST00000622427.4:c.63+53116G>A	ENSP00000483244.1:n.63+53116G>A
NM_001204403.1:c.96+95837G>A	NP_001191332.1:n.96+95837G>A
NM_001204404.1:c.63+53116G>A	NP_001191333.1:n.63+53116G>A
XM_011539700.1:c.102+95837G>A	XP_011538002.1:n.102+95837G>A
XM_011539701.1:c.96+95837G>A	XP_011538003.1:n.96+95837G>A
XM_011539702.1:c.57+213914G>A	XP_011538004.1:n.57+213914G>A
XM_017016114.1:c.63+53116G>A	XP_016871603.1:n.63+53116G>A
XM_024447958.1:c.63+53116G>A	XP_024303726.1:n.63+53116G>A
NM_001204403.2:c.96+95837G>A	NP_001191332.1:n.96+95837G>A
NM_001204404.2:c.63+53116G>A	NP_001191333.1:n.63+53116G>A