Canonical Allele Identifier: CA383456301
Gene: KCNA1 HGNC NCBI

Linked Data

dbSNP Id: rs104894352

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912601T>A , CM000674.2:g.4912601T>A GRCh38
NC_000012.11:g.5021767T>A , CM000674.1:g.5021767T>A GRCh37
NC_000012.10:g.4892028T>A NCBI36
NG_011815.1:g.7695T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.1223T>A MANE Select ENSP00000371985.3:p.Val408Glu
ENST00000543874.3:n.105+2129T>A
ENST00000639306.1:c.1061T>A ENSP00000492506.1:p.Val354Glu
ENST00000639680.1:c.76+335T>A
ENST00000382545.3:c.1223T>A ENSP00000371985.3:p.Val408Glu
ENST00000541095.1:n.105+2129T>A
ENST00000543874.2:n.96+2129T>A
NM_000217.2:c.1223T>A NP_000208.2:p.Val408Glu
NM_000217.3:c.1223T>A MANE Select NP_000208.2:p.Val408Glu