Canonical Allele Identifier: CA383466556
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2908857
ClinVar RCV Id: RCV003627396
dbSNP Id: rs1396628228
gnomAD v2: 12-5154780-C-G
gnomAD v4: 12-5045614-C-G
MyVariant Identifiers: chr12:g.5154780C>G (hg19) chr12:g.5045614C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045614C>G , CM000674.2:g.5045614C>G GRCh38
NC_000012.11:g.5154780C>G , CM000674.1:g.5154780C>G GRCh37
NC_000012.10:g.5025041C>G NCBI36
NG_012198.1:g.6696C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1467C>G MANE Select ENSP00000252321.3:p.Ile489Met
ENST00000252321.4:c.1467C>G ENSP00000252321.3:p.Ile489Met
NM_002234.3:c.1467C>G NP_002225.2:p.Ile489Met
NM_002234.4:c.1467C>G MANE Select NP_002225.2:p.Ile489Met
Search 100 bp 5'
Search 100 bp 3'