Canonical Allele Identifier: CA2013367711
Gene: KCNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4911972C= , CM000674.2:g.4911972C= GRCh38
NC_000012.11:g.5021138C= , CM000674.1:g.5021138C= GRCh37
NC_000012.10:g.4891399C= NCBI36
NG_011815.1:g.7066C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.594C= MANE Select ENSP00000371985.3:p.Phe198=
ENST00000543874.3:n.105+1500C=
ENST00000639306.1:c.432C= ENSP00000492506.1:p.Phe144=
ENST00000382545.3:c.594C= ENSP00000371985.3:p.Phe198=
ENST00000541095.1:n.105+1500C=
ENST00000543874.2:n.96+1500C=
NM_000217.2:c.594C= NP_000208.2:p.Phe198=
NM_000217.3:c.594C= MANE Select NP_000208.2:p.Phe198=