Canonical Allele Identifier: CA478094661
Gene: KCNA1 HGNC NCBI

Linked Data

gnomAD v4: 12-4912422-G-A
MyVariant Identifiers: chr12:g.5021588G>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912422G>A , CM000674.2:g.4912422G>A GRCh38
NC_000012.11:g.5021588G>A , CM000674.1:g.5021588G>A GRCh37
NC_000012.10:g.4891849G>A NCBI36
NG_011815.1:g.7516G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.1044G>A MANE Select ENSP00000371985.3:p.Glu348=
ENST00000543874.3:n.105+1950G>A
ENST00000639306.1:c.882G>A ENSP00000492506.1:p.Glu294=
ENST00000639680.1:c.76+156G>A
ENST00000382545.3:c.1044G>A ENSP00000371985.3:p.Glu348=
ENST00000541095.1:n.105+1950G>A
ENST00000543874.2:n.96+1950G>A
NM_000217.2:c.1044G>A NP_000208.2:p.Glu348=
NM_000217.3:c.1044G>A MANE Select NP_000208.2:p.Glu348=