Canonical Allele Identifier: CA6399775
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 498922
ClinVar RCV Id: RCV000596011
dbSNP Id: rs376977376
ExAC: 12:5154280 C / T
gnomAD v2: 12-5154280-C-T
gnomAD v3: 12-5045114-C-T
gnomAD v4: 12-5045114-C-T
MyVariant Identifiers: chr12:g.5154280C>T (hg19) chr12:g.5045114C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045114C>T , CM000674.2:g.5045114C>T GRCh38
NC_000012.11:g.5154280C>T , CM000674.1:g.5154280C>T GRCh37
NC_000012.10:g.5024541C>T NCBI36
NG_012198.1:g.6196C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252321.5:c.967C>T MANE Select ENSP00000252321.3:p.Pro323Ser
ENST00000252321.4:c.967C>T ENSP00000252321.3:p.Pro323Ser
NM_002234.3:c.967C>T NP_002225.2:p.Pro323Ser
NM_002234.4:c.967C>T MANE Select NP_002225.2:p.Pro323Ser
Search 100 bp 5'
Search 100 bp 3'