Canonical Allele Identifier: CA1188605063
Gene: KCNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672772C= , CM000663.2:g.110672772C= GRCh38
NC_000001.10:g.111215394C= , CM000663.1:g.111215394C= GRCh37
NC_000001.9:g.111016917C= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685980.2:c.*310G= ENSP00000513296.1:n.*310G=
ENST00000697409.1:c.*310G= ENSP00000513297.1:n.*310G=
ENST00000697410.1:c.*310G= ENSP00000513298.1:n.*310G=
ENST00000697411.1:c.1573+465G= ENSP00000513299.1:n.1573+465G=
ENST00000697412.1:c.*310G= ENSP00000513300.1:n.*310G=
ENST00000369769.4:c.*310G= MANE Select ENSP00000358784.2:n.*310G=
ENST00000369769.3:c.*310G= ENSP00000358784.2:n.*310G=
NM_002232.4:c.*310G= NP_002223.3:n.*310G=
NR_109845.1:n.218+465G=
XR_001738182.1:n.569-13602C=
XR_001738183.1:n.567-13602C=
XR_001738184.1:n.573-13602C=
XR_001738185.1:n.568-13602C=
XR_001738186.1:n.572-13602C=
XR_001738187.1:n.570-13602C=
NM_002232.5:c.*310G= MANE Select NP_002223.3:n.*310G=
NR_109845.2:n.218+465G=