Canonical Allele Identifier: CA2844772916
Gene: KCNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672812G>A , CM000663.2:g.110672812G>A GRCh38
NC_000001.10:g.111215434G>A , CM000663.1:g.111215434G>A GRCh37
NC_000001.9:g.111016957G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685980.2:c.*270C>T ENSP00000513296.1:n.*270C>T
ENST00000697409.1:c.*270C>T ENSP00000513297.1:n.*270C>T
ENST00000697410.1:c.*270C>T ENSP00000513298.1:n.*270C>T
ENST00000697411.1:c.1573+425C>T ENSP00000513299.1:n.1573+425C>T
ENST00000697412.1:c.*270C>T ENSP00000513300.1:n.*270C>T
ENST00000369769.4:c.*270C>T MANE Select ENSP00000358784.2:n.*270C>T
ENST00000369769.3:c.*270C>T ENSP00000358784.2:n.*270C>T
NM_002232.4:c.*270C>T NP_002223.3:n.*270C>T
NR_109845.1:n.218+425C>T
XR_001738182.1:n.569-13562G>A
XR_001738183.1:n.567-13562G>A
XR_001738184.1:n.573-13562G>A
XR_001738185.1:n.568-13562G>A
XR_001738186.1:n.572-13562G>A
XR_001738187.1:n.570-13562G>A
NM_002232.5:c.*270C>T MANE Select NP_002223.3:n.*270C>T
NR_109845.2:n.218+425C>T