Canonical Allele Identifier: CA383456228
Gene: KCNA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 431378
ClinVar RCV Id: RCV000496443
dbSNP Id: rs1135401950
MyVariant Identifiers: chr12:g.5021727G>T (hg19) chr12:g.4912561G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912561G>T , CM000674.2:g.4912561G>T GRCh38
NC_000012.11:g.5021727G>T , CM000674.1:g.5021727G>T GRCh37
NC_000012.10:g.4891988G>T NCBI36
NG_011815.1:g.7655G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.1183G>T MANE Select ENSP00000371985.3:p.Ala395Ser
ENST00000543874.3:n.105+2089G>T
ENST00000639306.1:c.1021G>T ENSP00000492506.1:p.Ala341Ser
ENST00000639680.1:c.76+295G>T
ENST00000382545.3:c.1183G>T ENSP00000371985.3:p.Ala395Ser
ENST00000541095.1:n.105+2089G>T
ENST00000543874.2:n.96+2089G>T
NM_000217.2:c.1183G>T NP_000208.2:p.Ala395Ser
NM_000217.3:c.1183G>T MANE Select NP_000208.2:p.Ala395Ser
Search 100 bp 5'
Search 100 bp 3'