Canonical Allele Identifier: CA1188605095
Gene: KCNA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.110672853_110672880delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG , CM000663.2:g.110672853_110672880delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG GRCh38
NC_000001.10:g.111215475_111215502delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG , CM000663.1:g.111215475_111215502delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG GRCh37
NC_000001.9:g.111016998_111017025delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000685980.2:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT ENSP00000513296.1:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCT...
ENST00000697409.1:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT ENSP00000513297.1:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCT...
ENST00000697410.1:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT ENSP00000513298.1:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCT...
ENST00000697411.1:c.1573+357_1573+384delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT ENSP00000513299.1:n.1573+357_1573+384delinsCTCTCCTTTTCCCTCTTA...
ENST00000697412.1:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT ENSP00000513300.1:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCT...
ENST00000369769.4:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT MANE Select ENSP00000358784.2:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCT...
ENST00000369769.3:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT ENSP00000358784.2:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCT...
NM_002232.4:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT NP_002223.3:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT
NR_109845.1:n.218+357_218+384delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT
XR_001738182.1:n.569-13521_569-13494delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG
XR_001738183.1:n.567-13521_567-13494delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG
XR_001738184.1:n.573-13521_573-13494delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG
XR_001738185.1:n.568-13521_568-13494delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG
XR_001738186.1:n.572-13521_572-13494delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG
XR_001738187.1:n.570-13521_570-13494delinsAGAGAGAGGGTAAGAGGGAAAAGGAGAG
NM_002232.5:c.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT MANE Select NP_002223.3:n.*202_*229delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT
NR_109845.2:n.218+357_218+384delinsCTCTCCTTTTCCCTCTTACCCTCTCTCT