Canonical Allele Identifier: CA2647068732

Gene: KCNA3

Linked Data

• gnomAD v4: 1-110672850-AAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672859_110672860del , CM000663.2:g.110672859_110672860del	GRCh38
NC_000001.10:g.111215481_111215482del , CM000663.1:g.111215481_111215482del	GRCh37
NC_000001.9:g.111017004_111017005del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685980.2:c.*230_*231del	ENSP00000513296.1:n.*230_*231del
ENST00000697409.1:c.*230_*231del	ENSP00000513297.1:n.*230_*231del
ENST00000697410.1:c.*230_*231del	ENSP00000513298.1:n.*230_*231del
ENST00000697411.1:c.1573+385_1573+386del	ENSP00000513299.1:n.1573+385_1573+386del
ENST00000697412.1:c.*230_*231del	ENSP00000513300.1:n.*230_*231del
ENST00000369769.4:c.*230_*231del MANE Select	ENSP00000358784.2:n.*230_*231del
ENST00000369769.3:c.*230_*231del	ENSP00000358784.2:n.*230_*231del
NM_002232.4:c.*230_*231del	NP_002223.3:n.*230_*231del
NR_109845.1:n.218+385_218+386del
XR_001738182.1:n.569-13515_569-13514del
XR_001738183.1:n.567-13515_567-13514del
XR_001738184.1:n.573-13515_573-13514del
XR_001738185.1:n.568-13515_568-13514del
XR_001738186.1:n.572-13515_572-13514del
XR_001738187.1:n.570-13515_570-13514del
NM_002232.5:c.*230_*231del MANE Select	NP_002223.3:n.*230_*231del
NR_109845.2:n.218+385_218+386del