Canonical Allele Identifier: CA1005713150

Gene: KCNA3

Linked Data

• dbSNP Id: rs1651936981
• gnomAD v3: 1-110672853-AGAGAGAGGGTAAGAGGGAAAAGGAGAG-A
• gnomAD v4: 1-110672853-AGAGAGAGGGTAAGAGGGAAAAGGAGAG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110672854_110672880del , CM000663.2:g.110672854_110672880del	GRCh38
NC_000001.10:g.111215476_111215502del , CM000663.1:g.111215476_111215502del	GRCh37
NC_000001.9:g.111016999_111017025del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685980.2:c.*202_*228del	ENSP00000513296.1:n.*202_*228del
ENST00000697409.1:c.*202_*228del	ENSP00000513297.1:n.*202_*228del
ENST00000697410.1:c.*202_*228del	ENSP00000513298.1:n.*202_*228del
ENST00000697411.1:c.1573+357_1573+383del	ENSP00000513299.1:n.1573+357_1573+383del
ENST00000697412.1:c.*202_*228del	ENSP00000513300.1:n.*202_*228del
ENST00000369769.4:c.*202_*228del MANE Select	ENSP00000358784.2:n.*202_*228del
ENST00000369769.3:c.*202_*228del	ENSP00000358784.2:n.*202_*228del
NM_002232.4:c.*202_*228del	NP_002223.3:n.*202_*228del
NR_109845.1:n.218+357_218+383del
XR_001738182.1:n.569-13520_569-13494del
XR_001738183.1:n.567-13520_567-13494del
XR_001738184.1:n.573-13520_573-13494del
XR_001738185.1:n.568-13520_568-13494del
XR_001738186.1:n.572-13520_572-13494del
XR_001738187.1:n.570-13520_570-13494del
NM_002232.5:c.*202_*228del MANE Select	NP_002223.3:n.*202_*228del
NR_109845.2:n.218+357_218+383del