Canonical Allele Identifier: CA383454725
Gene: KCNA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2131742
ClinVar RCV Id: RCV003036405
MyVariant Identifiers: chr12:g.5021055A>G (hg19) chr12:g.4911889A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4911889A>G , CM000674.2:g.4911889A>G GRCh38
NC_000012.11:g.5021055A>G , CM000674.1:g.5021055A>G GRCh37
NC_000012.10:g.4891316A>G NCBI36
NG_011815.1:g.6983A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.511A>G MANE Select ENSP00000371985.3:p.Ile171Val
ENST00000543874.3:n.105+1417A>G
ENST00000639306.1:c.349A>G ENSP00000492506.1:p.Ile117Val
ENST00000382545.3:c.511A>G ENSP00000371985.3:p.Ile171Val
ENST00000541095.1:n.105+1417A>G
ENST00000543874.2:n.96+1417A>G
NM_000217.2:c.511A>G NP_000208.2:p.Ile171Val
NM_000217.3:c.511A>G MANE Select NP_000208.2:p.Ile171Val
Search 100 bp 5'
Search 100 bp 3'