Canonical Allele Identifier: CA1188605072
Gene: KCNA3 HGNC NCBI

Linked Data

dbSNP Id: rs1651933961

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672788_110672789del , CM000663.2:g.110672788_110672789del GRCh38
NC_000001.10:g.111215410_111215411del , CM000663.1:g.111215410_111215411del GRCh37
NC_000001.9:g.111016933_111016934del NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000685980.2:c.*295_*296del ENSP00000513296.1:n.*295_*296del
ENST00000697409.1:c.*295_*296del ENSP00000513297.1:n.*295_*296del
ENST00000697410.1:c.*295_*296del ENSP00000513298.1:n.*295_*296del
ENST00000697411.1:c.1573+450_1573+451del ENSP00000513299.1:n.1573+450_1573+451del
ENST00000697412.1:c.*295_*296del ENSP00000513300.1:n.*295_*296del
ENST00000369769.4:c.*295_*296del MANE Select ENSP00000358784.2:n.*295_*296del
ENST00000369769.3:c.*295_*296del ENSP00000358784.2:n.*295_*296del
NM_002232.4:c.*295_*296del NP_002223.3:n.*295_*296del
NR_109845.1:n.218+450_218+451del
XR_001738182.1:n.569-13586_569-13585del
XR_001738183.1:n.567-13586_567-13585del
XR_001738184.1:n.573-13586_573-13585del
XR_001738185.1:n.568-13586_568-13585del
XR_001738186.1:n.572-13586_572-13585del
XR_001738187.1:n.570-13586_570-13585del
NM_002232.5:c.*295_*296del MANE Select NP_002223.3:n.*295_*296del
NR_109845.2:n.218+450_218+451del