Canonical Allele Identifier: CA2013367895
Gene: KCNA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912500A= , CM000674.2:g.4912500A= GRCh38
NC_000012.11:g.5021666A= , CM000674.1:g.5021666A= GRCh37
NC_000012.10:g.4891927A= NCBI36
NG_011815.1:g.7594A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.1122A= MANE Select ENSP00000371985.3:p.Gly374=
ENST00000543874.3:n.105+2028A=
ENST00000639306.1:c.960A= ENSP00000492506.1:p.Gly320=
ENST00000639680.1:c.76+234A=
ENST00000382545.3:c.1122A= ENSP00000371985.3:p.Gly374=
ENST00000541095.1:n.105+2028A=
ENST00000543874.2:n.96+2028A=
NM_000217.2:c.1122A= NP_000208.2:p.Gly374=
NM_000217.3:c.1122A= MANE Select NP_000208.2:p.Gly374=