Canonical Allele Identifier: CA885466441

Gene: KCNA3

Linked Data

• dbSNP Id: rs1433534903
• MyVariant Identifiers: chr1:g.111215471_111215484del (hg19) ; chr1:g.110672849_110672862del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672855_110672868del , CM000663.2:g.110672855_110672868del	GRCh38
NC_000001.10:g.111215477_111215490del , CM000663.1:g.111215477_111215490del	GRCh37
NC_000001.9:g.111017000_111017013del	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000685980.2:c.*220_*233del	ENSP00000513296.1:n.*220_*233del
ENST00000697409.1:c.*220_*233del	ENSP00000513297.1:n.*220_*233del
ENST00000697410.1:c.*220_*233del	ENSP00000513298.1:n.*220_*233del
ENST00000697411.1:c.1573+375_1573+388del	ENSP00000513299.1:n.1573+375_1573+388del
ENST00000697412.1:c.*220_*233del	ENSP00000513300.1:n.*220_*233del
ENST00000369769.4:c.*220_*233del MANE Select	ENSP00000358784.2:n.*220_*233del
ENST00000369769.3:c.*220_*233del	ENSP00000358784.2:n.*220_*233del
NM_002232.4:c.*220_*233del	NP_002223.3:n.*220_*233del
NR_109845.1:n.218+375_218+388del
XR_001738182.1:n.569-13519_569-13506del
XR_001738183.1:n.567-13519_567-13506del
XR_001738184.1:n.573-13519_573-13506del
XR_001738185.1:n.568-13519_568-13506del
XR_001738186.1:n.572-13519_572-13506del
XR_001738187.1:n.570-13519_570-13506del
NM_002232.5:c.*220_*233del MANE Select	NP_002223.3:n.*220_*233del
NR_109845.2:n.218+375_218+388del