Canonical Allele Identifier: CA6399398
Gene: KCNA1 HGNC NCBI

Linked Data

dbSNP Id: rs779656199
ExAC: 12:5021058 G / A
gnomAD v2: 12-5021058-G-A
gnomAD v4: 12-4911892-G-A
COSMIC: COSM4749122
MyVariant Identifiers: chr12:g.5021058G>A (hg19) chr12:g.4911892G>A (hg38)
PubMed: PMID:28135719
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4911892G>A , CM000674.2:g.4911892G>A GRCh38
NC_000012.11:g.5021058G>A , CM000674.1:g.5021058G>A GRCh37
NC_000012.10:g.4891319G>A NCBI36
NG_011815.1:g.6986G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.514G>A MANE Select ENSP00000371985.3:p.Val172Ile
ENST00000543874.3:n.105+1420G>A
ENST00000639306.1:c.352G>A ENSP00000492506.1:p.Val118Ile
ENST00000382545.3:c.514G>A ENSP00000371985.3:p.Val172Ile
ENST00000541095.1:n.105+1420G>A
ENST00000543874.2:n.96+1420G>A
NM_000217.2:c.514G>A NP_000208.2:p.Val172Ile
NM_000217.3:c.514G>A MANE Select NP_000208.2:p.Val172Ile
Search 100 bp 5'
Search 100 bp 3'