Canonical Allele Identifier: CA383467052
Gene: KCNA5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5155019C>G (hg19) chr12:g.5045853C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045853C>G , CM000674.2:g.5045853C>G GRCh38
NC_000012.11:g.5155019C>G , CM000674.1:g.5155019C>G GRCh37
NC_000012.10:g.5025280C>G NCBI36
NG_012198.1:g.6935C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252321.5:c.1706C>G MANE Select ENSP00000252321.3:p.Thr569Ser
ENST00000252321.4:c.1706C>G ENSP00000252321.3:p.Thr569Ser
NM_002234.3:c.1706C>G NP_002225.2:p.Thr569Ser
NM_002234.4:c.1706C>G MANE Select NP_002225.2:p.Thr569Ser
Search 100 bp 5'
Search 100 bp 3'