Canonical Allele Identifier: CA383464966
Gene: KCNA5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5154008T>A (hg19) chr12:g.5044842T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044842T>A , CM000674.2:g.5044842T>A GRCh38
NC_000012.11:g.5154008T>A , CM000674.1:g.5154008T>A GRCh37
NC_000012.10:g.5024269T>A NCBI36
NG_012198.1:g.5924T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.695T>A MANE Select ENSP00000252321.3:p.Phe232Tyr
ENST00000252321.4:c.695T>A ENSP00000252321.3:p.Phe232Tyr
NM_002234.3:c.695T>A NP_002225.2:p.Phe232Tyr
NM_002234.4:c.695T>A MANE Select NP_002225.2:p.Phe232Tyr
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