Canonical Allele Identifier: CA2580060797

Gene: KCNA3

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110673407_110673408delinsAA , CM000663.2:g.110673407_110673408delinsAA	GRCh38
NC_000001.10:g.111216029_111216030delinsAA , CM000663.1:g.111216029_111216030delinsAA	GRCh37
NC_000001.9:g.111017552_111017553delinsAA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_002232.5:c.1402_1403delinsTT MANE Select	NP_002223.3:p.Gly468Phe
ENST00000369769.4:c.1402_1403delinsTT MANE Select	ENSP00000358784.2:p.Gly468Phe
NM_002232.4:c.1402_1403delinsTT	NP_002223.3:p.Gly468Phe
NR_109845.1:n.47_48delinsTT
NR_109845.2:n.47_48delinsTT
ENST00000369769.3:c.1402_1403delinsTT	ENSP00000358784.2:p.Gly468Phe
ENST00000685980.2:c.1402_1403delinsTT	ENSP00000513296.1:p.Gly468Phe
ENST00000697409.1:c.1402_1403delinsTT	ENSP00000513297.1:p.Gly468Phe
ENST00000697410.1:c.1402_1403delinsTT	ENSP00000513298.1:p.Gly468Phe
ENST00000697411.1:c.1402_1403delinsTT	ENSP00000513299.1:p.Gly468Phe
ENST00000697412.1:c.1402_1403delinsTT	ENSP00000513300.1:p.Gly468Phe
XR_001738182.1:n.569-12967_569-12966delinsAA
XR_001738183.1:n.567-12967_567-12966delinsAA
XR_001738184.1:n.573-12967_573-12966delinsAA
XR_001738185.1:n.568-12967_568-12966delinsAA
XR_001738186.1:n.572-12967_572-12966delinsAA
XR_001738187.1:n.570-12967_570-12966delinsAA