Canonical Allele Identifier: CA2013367727
Gene: KCNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912005G= , CM000674.2:g.4912005G= GRCh38
NC_000012.11:g.5021171G= , CM000674.1:g.5021171G= GRCh37
NC_000012.10:g.4891432G= NCBI36
NG_011815.1:g.7099G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.627G= MANE Select ENSP00000371985.3:p.Thr209=
ENST00000543874.3:n.105+1533G=
ENST00000639306.1:c.465G= ENSP00000492506.1:p.Thr155=
ENST00000382545.3:c.627G= ENSP00000371985.3:p.Thr209=
ENST00000541095.1:n.105+1533G=
ENST00000543874.2:n.96+1533G=
NM_000217.2:c.627G= NP_000208.2:p.Thr209=
NM_000217.3:c.627G= MANE Select NP_000208.2:p.Thr209=