Canonical Allele Identifier: CA2561197533
Gene: ANK3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.60421383T>A , CM000672.2:g.60421383T>A GRCh38
NC_000010.10:g.62181141T>A , CM000672.1:g.62181141T>A GRCh37
NC_000010.9:g.61851147T>A NCBI36
NG_029917.1:g.317144A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000503366.6:c.64-141744A>T ENSP00000425236.1:n.64-141744A>T
ENST00000373827.6:c.97-141744A>T ENSP00000362933.2:n.97-141744A>T
ENST00000503366.5:c.64-141744A>T ENSP00000425236.1:n.64-141744A>T
ENST00000622427.4:c.64-141744A>T ENSP00000483244.1:n.64-141744A>T
NM_001204403.1:c.97-141744A>T NP_001191332.1:n.97-141744A>T
NM_001204404.1:c.64-141744A>T NP_001191333.1:n.64-141744A>T
XM_011539700.1:c.103-141744A>T XP_011538002.1:n.103-141744A>T
XM_011539701.1:c.97-141744A>T XP_011538003.1:n.97-141744A>T
XM_011539702.1:c.58-141744A>T XP_011538004.1:n.58-141744A>T
XM_011539704.1:c.15+76601A>T XP_011538006.1:n.15+76601A>T
XM_017016114.1:c.64-141744A>T XP_016871603.1:n.64-141744A>T
XM_024447958.1:c.64-141744A>T XP_024303726.1:n.64-141744A>T
NM_001204403.2:c.97-141744A>T NP_001191332.1:n.97-141744A>T
NM_001204404.2:c.64-141744A>T NP_001191333.1:n.64-141744A>T