Canonical Allele Identifier: CA2647068708

Gene: KCNA3

Linked Data

• gnomAD v4: 1-110672840-TTA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672841_110672842del , CM000663.2:g.110672841_110672842del	GRCh38
NC_000001.10:g.111215463_111215464del , CM000663.1:g.111215463_111215464del	GRCh37
NC_000001.9:g.111016986_111016987del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685980.2:c.*240_*241del	ENSP00000513296.1:n.*240_*241del
ENST00000697409.1:c.*240_*241del	ENSP00000513297.1:n.*240_*241del
ENST00000697410.1:c.*240_*241del	ENSP00000513298.1:n.*240_*241del
ENST00000697411.1:c.1573+395_1573+396del	ENSP00000513299.1:n.1573+395_1573+396del
ENST00000697412.1:c.*240_*241del	ENSP00000513300.1:n.*240_*241del
ENST00000369769.4:c.*240_*241del MANE Select	ENSP00000358784.2:n.*240_*241del
ENST00000369769.3:c.*240_*241del	ENSP00000358784.2:n.*240_*241del
NM_002232.4:c.*240_*241del	NP_002223.3:n.*240_*241del
NR_109845.1:n.218+395_218+396del
XR_001738182.1:n.569-13533_569-13532del
XR_001738183.1:n.567-13533_567-13532del
XR_001738184.1:n.573-13533_573-13532del
XR_001738185.1:n.568-13533_568-13532del
XR_001738186.1:n.572-13533_572-13532del
XR_001738187.1:n.570-13533_570-13532del
NM_002232.5:c.*240_*241del MANE Select	NP_002223.3:n.*240_*241del
NR_109845.2:n.218+395_218+396del