Canonical Allele Identifier: CA478095672
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1093981
ClinVar RCV Id: RCV001414296
dbSNP Id: rs781723666
MyVariant Identifiers: chr12:g.5154555C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045389C>T , CM000674.2:g.5045389C>T GRCh38
NC_000012.11:g.5154555C>T , CM000674.1:g.5154555C>T GRCh37
NC_000012.10:g.5024816C>T NCBI36
NG_012198.1:g.6471C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1242C>T MANE Select ENSP00000252321.3:p.Ser414=
ENST00000252321.4:c.1242C>T ENSP00000252321.3:p.Ser414=
NM_002234.3:c.1242C>T NP_002225.2:p.Ser414=
NM_002234.4:c.1242C>T MANE Select NP_002225.2:p.Ser414=
Search 100 bp 5'
Search 100 bp 3'