Canonical Allele Identifier: CA593963934

Gene: ANK3

Linked Data

• dbSNP Id: rs1386803614
• gnomAD v2: 10-62181163-A-C
• MyVariant Identifiers: chr10:g.62181163A>C (hg19) ; chr10:g.60421405A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.60421405A>C , CM000672.2:g.60421405A>C	GRCh38
NC_000010.10:g.62181163A>C , CM000672.1:g.62181163A>C	GRCh37
NC_000010.9:g.61851169A>C	NCBI36
NG_029917.1:g.317122T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000503366.6:c.64-141766T>G	ENSP00000425236.1:n.64-141766T>G
ENST00000373827.6:c.97-141766T>G	ENSP00000362933.2:n.97-141766T>G
ENST00000503366.5:c.64-141766T>G	ENSP00000425236.1:n.64-141766T>G
ENST00000622427.4:c.64-141766T>G	ENSP00000483244.1:n.64-141766T>G
NM_001204403.1:c.97-141766T>G	NP_001191332.1:n.97-141766T>G
NM_001204404.1:c.64-141766T>G	NP_001191333.1:n.64-141766T>G
XM_011539700.1:c.103-141766T>G	XP_011538002.1:n.103-141766T>G
XM_011539701.1:c.97-141766T>G	XP_011538003.1:n.97-141766T>G
XM_011539702.1:c.58-141766T>G	XP_011538004.1:n.58-141766T>G
XM_011539704.1:c.15+76579T>G	XP_011538006.1:n.15+76579T>G
XM_017016114.1:c.64-141766T>G	XP_016871603.1:n.64-141766T>G
XM_024447958.1:c.64-141766T>G	XP_024303726.1:n.64-141766T>G
NM_001204403.2:c.97-141766T>G	NP_001191332.1:n.97-141766T>G
NM_001204404.2:c.64-141766T>G	NP_001191333.1:n.64-141766T>G