Canonical Allele Identifier: CA6399475
Gene: KCNA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1630184
ClinVar RCV Id: RCV002120992
dbSNP Id: rs138936640
ExAC: 12:5021765 T / C
gnomAD v2: 12-5021765-T-C
gnomAD v3: 12-4912599-T-C
gnomAD v4: 12-4912599-T-C
MyVariant Identifiers: chr12:g.5021765T>C (hg19) chr12:g.4912599T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912599T>C , CM000674.2:g.4912599T>C GRCh38
NC_000012.11:g.5021765T>C , CM000674.1:g.5021765T>C GRCh37
NC_000012.10:g.4892026T>C NCBI36
NG_011815.1:g.7693T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.1221T>C MANE Select ENSP00000371985.3:p.Ile407=
ENST00000543874.3:n.105+2127T>C
ENST00000639306.1:c.1059T>C ENSP00000492506.1:p.Ile353=
ENST00000639680.1:c.76+333T>C
ENST00000382545.3:c.1221T>C ENSP00000371985.3:p.Ile407=
ENST00000541095.1:n.105+2127T>C
ENST00000543874.2:n.96+2127T>C
NM_000217.2:c.1221T>C NP_000208.2:p.Ile407=
NM_000217.3:c.1221T>C MANE Select NP_000208.2:p.Ile407=
Search 100 bp 5'
Search 100 bp 3'