Canonical Allele Identifier: CA1188605093
Gene: KCNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672848_110672862delinsTTAAGAGAGAGAGGG , CM000663.2:g.110672848_110672862delinsTTAAGAGAGAGAGGG GRCh38
NC_000001.10:g.111215470_111215484delinsTTAAGAGAGAGAGGG , CM000663.1:g.111215470_111215484delinsTTAAGAGAGAGAGGG GRCh37
NC_000001.9:g.111016993_111017007delinsTTAAGAGAGAGAGGG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685980.2:c.*220_*234delinsCCCTCTCTCTCTTAA ENSP00000513296.1:n.*220_*234delinsCCCTCTCTCTCTTAA
ENST00000697409.1:c.*220_*234delinsCCCTCTCTCTCTTAA ENSP00000513297.1:n.*220_*234delinsCCCTCTCTCTCTTAA
ENST00000697410.1:c.*220_*234delinsCCCTCTCTCTCTTAA ENSP00000513298.1:n.*220_*234delinsCCCTCTCTCTCTTAA
ENST00000697411.1:c.1573+375_1573+389delinsCCCTCTCTCTCTTAA ENSP00000513299.1:n.1573+375_1573+389delinsCCCTCTCTCTCTTAA
ENST00000697412.1:c.*220_*234delinsCCCTCTCTCTCTTAA ENSP00000513300.1:n.*220_*234delinsCCCTCTCTCTCTTAA
ENST00000369769.4:c.*220_*234delinsCCCTCTCTCTCTTAA MANE Select ENSP00000358784.2:n.*220_*234delinsCCCTCTCTCTCTTAA
ENST00000369769.3:c.*220_*234delinsCCCTCTCTCTCTTAA ENSP00000358784.2:n.*220_*234delinsCCCTCTCTCTCTTAA
NM_002232.4:c.*220_*234delinsCCCTCTCTCTCTTAA NP_002223.3:n.*220_*234delinsCCCTCTCTCTCTTAA
NR_109845.1:n.218+375_218+389delinsCCCTCTCTCTCTTAA
XR_001738182.1:n.569-13526_569-13512delinsTTAAGAGAGAGAGGG
XR_001738183.1:n.567-13526_567-13512delinsTTAAGAGAGAGAGGG
XR_001738184.1:n.573-13526_573-13512delinsTTAAGAGAGAGAGGG
XR_001738185.1:n.568-13526_568-13512delinsTTAAGAGAGAGAGGG
XR_001738186.1:n.572-13526_572-13512delinsTTAAGAGAGAGAGGG
XR_001738187.1:n.570-13526_570-13512delinsTTAAGAGAGAGAGGG
NM_002232.5:c.*220_*234delinsCCCTCTCTCTCTTAA MANE Select NP_002223.3:n.*220_*234delinsCCCTCTCTCTCTTAA
NR_109845.2:n.218+375_218+389delinsCCCTCTCTCTCTTAA