Canonical Allele Identifier: CA667056779

Gene: ANK3

Linked Data

• dbSNP Id: rs890573669
• gnomAD v3: 10-60462435-G-A
• gnomAD v4: 10-60462435-G-A
• MyVariant Identifiers: chr10:g.62222193G>A (hg19) ; chr10:g.60462435G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60462435G>A , CM000672.2:g.60462435G>A	GRCh38
NC_000010.10:g.62222193G>A , CM000672.1:g.62222193G>A	GRCh37
NC_000010.9:g.61892199G>A	NCBI36
NG_029917.1:g.276092C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000503366.6:c.63+110030C>T	ENSP00000425236.1:n.63+110030C>T
ENST00000373827.6:c.96+152751C>T	ENSP00000362933.2:n.96+152751C>T
ENST00000503366.5:c.63+110030C>T	ENSP00000425236.1:n.63+110030C>T
ENST00000622427.4:c.63+110030C>T	ENSP00000483244.1:n.63+110030C>T
NM_001204403.1:c.96+152751C>T	NP_001191332.1:n.96+152751C>T
NM_001204404.1:c.63+110030C>T	NP_001191333.1:n.63+110030C>T
XM_011539700.1:c.102+152751C>T	XP_011538002.1:n.102+152751C>T
XM_011539701.1:c.96+152751C>T	XP_011538003.1:n.96+152751C>T
XM_011539702.1:c.58-182796C>T	XP_011538004.1:n.58-182796C>T
XM_011539704.1:c.15+35549C>T	XP_011538006.1:n.15+35549C>T
XM_017016114.1:c.63+110030C>T	XP_016871603.1:n.63+110030C>T
XM_024447958.1:c.63+110030C>T	XP_024303726.1:n.63+110030C>T
NM_001204403.2:c.96+152751C>T	NP_001191332.1:n.96+152751C>T
NM_001204404.2:c.63+110030C>T	NP_001191333.1:n.63+110030C>T