Canonical Allele Identifier: CA2013367805
Gene: KCNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912191C= , CM000674.2:g.4912191C= GRCh38
NC_000012.11:g.5021357C= , CM000674.1:g.5021357C= GRCh37
NC_000012.10:g.4891618C= NCBI36
NG_011815.1:g.7285C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.813C= MANE Select ENSP00000371985.3:p.Thr271=
ENST00000543874.3:n.105+1719C=
ENST00000639306.1:c.651C= ENSP00000492506.1:p.Thr217=
ENST00000639680.1:c.1C=
ENST00000382545.3:c.813C= ENSP00000371985.3:p.Thr271=
ENST00000541095.1:n.105+1719C=
ENST00000543874.2:n.96+1719C=
NM_000217.2:c.813C= NP_000208.2:p.Thr271=
NM_000217.3:c.813C= MANE Select NP_000208.2:p.Thr271=