Canonical Allele Identifier: CA2013367726
Gene: KCNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912004C= , CM000674.2:g.4912004C= GRCh38
NC_000012.11:g.5021170C= , CM000674.1:g.5021170C= GRCh37
NC_000012.10:g.4891431C= NCBI36
NG_011815.1:g.7098C=

Transcript Alleles

HGVS Amino-acid change
ENST00000382545.5:c.626C= MANE Select ENSP00000371985.3:p.Thr209=
ENST00000543874.3:n.105+1532C=
ENST00000639306.1:c.464C= ENSP00000492506.1:p.Thr155=
ENST00000382545.3:c.626C= ENSP00000371985.3:p.Thr209=
ENST00000541095.1:n.105+1532C=
ENST00000543874.2:n.96+1532C=
NM_000217.2:c.626C= NP_000208.2:p.Thr209=
NM_000217.3:c.626C= MANE Select NP_000208.2:p.Thr209=