Canonical Allele Identifier: CA1188605070
Gene: KCNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672784T= , CM000663.2:g.110672784T= GRCh38
NC_000001.10:g.111215406T= , CM000663.1:g.111215406T= GRCh37
NC_000001.9:g.111016929T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685980.2:c.*298A= ENSP00000513296.1:n.*298A=
ENST00000697409.1:c.*298A= ENSP00000513297.1:n.*298A=
ENST00000697410.1:c.*298A= ENSP00000513298.1:n.*298A=
ENST00000697411.1:c.1573+453A= ENSP00000513299.1:n.1573+453A=
ENST00000697412.1:c.*298A= ENSP00000513300.1:n.*298A=
ENST00000369769.4:c.*298A= MANE Select ENSP00000358784.2:n.*298A=
ENST00000369769.3:c.*298A= ENSP00000358784.2:n.*298A=
NM_002232.4:c.*298A= NP_002223.3:n.*298A=
NR_109845.1:n.218+453A=
XR_001738182.1:n.569-13590T=
XR_001738183.1:n.567-13590T=
XR_001738184.1:n.573-13590T=
XR_001738185.1:n.568-13590T=
XR_001738186.1:n.572-13590T=
XR_001738187.1:n.570-13590T=
NM_002232.5:c.*298A= MANE Select NP_002223.3:n.*298A=
NR_109845.2:n.218+453A=