Canonical Allele Identifier: CA383464828
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1010338
ClinVar RCV Id: RCV001307949
dbSNP Id: rs1862753153
gnomAD v4: 12-5044778-G-C
MyVariant Identifiers: chr12:g.5153944G>C (hg19) chr12:g.5044778G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044778G>C , CM000674.2:g.5044778G>C GRCh38
NC_000012.11:g.5153944G>C , CM000674.1:g.5153944G>C GRCh37
NC_000012.10:g.5024205G>C NCBI36
NG_012198.1:g.5860G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.631G>C MANE Select ENSP00000252321.3:p.Glu211Gln
ENST00000252321.4:c.631G>C ENSP00000252321.3:p.Glu211Gln
NM_002234.3:c.631G>C NP_002225.2:p.Glu211Gln
NM_002234.4:c.631G>C MANE Select NP_002225.2:p.Glu211Gln
Search 100 bp 5'
Search 100 bp 3'