Canonical Allele Identifier: CA1188605071

Gene: KCNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672785_110672787delinsGCT , CM000663.2:g.110672785_110672787delinsGCT	GRCh38
NC_000001.10:g.111215407_111215409delinsGCT , CM000663.1:g.111215407_111215409delinsGCT	GRCh37
NC_000001.9:g.111016930_111016932delinsGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685980.2:c.*295_*297delinsAGC	ENSP00000513296.1:n.*295_*297delinsAGC
ENST00000697409.1:c.*295_*297delinsAGC	ENSP00000513297.1:n.*295_*297delinsAGC
ENST00000697410.1:c.*295_*297delinsAGC	ENSP00000513298.1:n.*295_*297delinsAGC
ENST00000697411.1:c.1573+450_1573+452delinsAGC	ENSP00000513299.1:n.1573+450_1573+452deli...
ENST00000697412.1:c.*295_*297delinsAGC	ENSP00000513300.1:n.*295_*297delinsAGC
ENST00000369769.4:c.*295_*297delinsAGC MANE Select	ENSP00000358784.2:n.*295_*297delinsAGC
ENST00000369769.3:c.*295_*297delinsAGC	ENSP00000358784.2:n.*295_*297delinsAGC
NM_002232.4:c.*295_*297delinsAGC	NP_002223.3:n.*295_*297delinsAGC
NR_109845.1:n.218+450_218+452delinsAGC
XR_001738182.1:n.569-13589_569-13587delinsGCT
XR_001738183.1:n.567-13589_567-13587delinsGCT
XR_001738184.1:n.573-13589_573-13587delinsGCT
XR_001738185.1:n.568-13589_568-13587delinsGCT
XR_001738186.1:n.572-13589_572-13587delinsGCT
XR_001738187.1:n.570-13589_570-13587delinsGCT
NM_002232.5:c.*295_*297delinsAGC MANE Select	NP_002223.3:n.*295_*297delinsAGC
NR_109845.2:n.218+450_218+452delinsAGC