Canonical Allele Identifier: CA6399828
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1018732
ClinVar RCV Id: RCV001318072
dbSNP Id: rs763570659
ExAC: 12:5154538 C / T
gnomAD v3: 12-5045372-C-T
gnomAD v4: 12-5045372-C-T
MyVariant Identifiers: chr12:g.5154538C>T (hg19) chr12:g.5045372C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045372C>T , CM000674.2:g.5045372C>T GRCh38
NC_000012.11:g.5154538C>T , CM000674.1:g.5154538C>T GRCh37
NC_000012.10:g.5024799C>T NCBI36
NG_012198.1:g.6454C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1225C>T MANE Select ENSP00000252321.3:p.Arg409Cys
ENST00000252321.4:c.1225C>T ENSP00000252321.3:p.Arg409Cys
NM_002234.3:c.1225C>T NP_002225.2:p.Arg409Cys
NM_002234.4:c.1225C>T MANE Select NP_002225.2:p.Arg409Cys
Search 100 bp 5'
Search 100 bp 3'