Canonical Allele Identifier: CA383466200
Gene: KCNA5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5154619C>G (hg19) chr12:g.5045453C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045453C>G , CM000674.2:g.5045453C>G GRCh38
NC_000012.11:g.5154619C>G , CM000674.1:g.5154619C>G GRCh37
NC_000012.10:g.5024880C>G NCBI36
NG_012198.1:g.6535C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1306C>G MANE Select ENSP00000252321.3:p.Leu436Val
ENST00000252321.4:c.1306C>G ENSP00000252321.3:p.Leu436Val
NM_002234.3:c.1306C>G NP_002225.2:p.Leu436Val
NM_002234.4:c.1306C>G MANE Select NP_002225.2:p.Leu436Val
Search 100 bp 5'
Search 100 bp 3'