Canonical Allele Identifier: CA667040880

Gene: ANK3

Linked Data

• dbSNP Id: rs1305099685
• MyVariant Identifiers: chr10:g.62185379G>C (hg19) ; chr10:g.60425621G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60425621G>C , CM000672.2:g.60425621G>C	GRCh38
NC_000010.10:g.62185379G>C , CM000672.1:g.62185379G>C	GRCh37
NC_000010.9:g.61855385G>C	NCBI36
NG_029917.1:g.312906C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000503366.6:c.64-145982C>G	ENSP00000425236.1:n.64-145982C>G
ENST00000373827.6:c.97-145982C>G	ENSP00000362933.2:n.97-145982C>G
ENST00000503366.5:c.64-145982C>G	ENSP00000425236.1:n.64-145982C>G
ENST00000622427.4:c.64-145982C>G	ENSP00000483244.1:n.64-145982C>G
NM_001204403.1:c.97-145982C>G	NP_001191332.1:n.97-145982C>G
NM_001204404.1:c.64-145982C>G	NP_001191333.1:n.64-145982C>G
XM_011539700.1:c.103-145982C>G	XP_011538002.1:n.103-145982C>G
XM_011539701.1:c.97-145982C>G	XP_011538003.1:n.97-145982C>G
XM_011539702.1:c.58-145982C>G	XP_011538004.1:n.58-145982C>G
XM_011539704.1:c.15+72363C>G	XP_011538006.1:n.15+72363C>G
XM_017016114.1:c.64-145982C>G	XP_016871603.1:n.64-145982C>G
XM_024447958.1:c.64-145982C>G	XP_024303726.1:n.64-145982C>G
NM_001204403.2:c.97-145982C>G	NP_001191332.1:n.97-145982C>G
NM_001204404.2:c.64-145982C>G	NP_001191333.1:n.64-145982C>G