Canonical Allele Identifier: CA383456282
Gene: KCNA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 985808
ClinVar RCV Id: RCV001266903 RCV002290674
dbSNP Id: rs1947358808
MyVariant Identifiers: chr12:g.5021757C>G (hg19) chr12:g.4912591C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912591C>G , CM000674.2:g.4912591C>G GRCh38
NC_000012.11:g.5021757C>G , CM000674.1:g.5021757C>G GRCh37
NC_000012.10:g.4892018C>G NCBI36
NG_011815.1:g.7685C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.1213C>G MANE Select ENSP00000371985.3:p.Pro405Ala
ENST00000543874.3:n.105+2119C>G
ENST00000639306.1:c.1051C>G ENSP00000492506.1:p.Pro351Ala
ENST00000639680.1:c.76+325C>G
ENST00000382545.3:c.1213C>G ENSP00000371985.3:p.Pro405Ala
ENST00000541095.1:n.105+2119C>G
ENST00000543874.2:n.96+2119C>G
NM_000217.2:c.1213C>G NP_000208.2:p.Pro405Ala
NM_000217.3:c.1213C>G MANE Select NP_000208.2:p.Pro405Ala
Search 100 bp 5'
Search 100 bp 3'