Canonical Allele Identifier: CA208323154

Gene: ANK3

Linked Data

• dbSNP Id: rs1012441230
• MyVariant Identifiers: chr10:g.62179750C>A (hg19) ; chr10:g.60419992C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60419992C>A , CM000672.2:g.60419992C>A	GRCh38
NC_000010.10:g.62179750C>A , CM000672.1:g.62179750C>A	GRCh37
NC_000010.9:g.61849756C>A	NCBI36
NG_029917.1:g.318535G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000503366.6:c.64-140353G>T	ENSP00000425236.1:n.64-140353G>T
ENST00000373827.6:c.97-140353G>T	ENSP00000362933.2:n.97-140353G>T
ENST00000503366.5:c.64-140353G>T	ENSP00000425236.1:n.64-140353G>T
ENST00000622427.4:c.64-140353G>T	ENSP00000483244.1:n.64-140353G>T
NM_001204403.1:c.97-140353G>T	NP_001191332.1:n.97-140353G>T
NM_001204404.1:c.64-140353G>T	NP_001191333.1:n.64-140353G>T
XM_011539700.1:c.103-140353G>T	XP_011538002.1:n.103-140353G>T
XM_011539701.1:c.97-140353G>T	XP_011538003.1:n.97-140353G>T
XM_011539702.1:c.58-140353G>T	XP_011538004.1:n.58-140353G>T
XM_011539704.1:c.15+77992G>T	XP_011538006.1:n.15+77992G>T
XM_017016114.1:c.64-140353G>T	XP_016871603.1:n.64-140353G>T
XM_024447958.1:c.64-140353G>T	XP_024303726.1:n.64-140353G>T
NM_001204403.2:c.97-140353G>T	NP_001191332.1:n.97-140353G>T
NM_001204404.2:c.64-140353G>T	NP_001191333.1:n.64-140353G>T