Canonical Allele Identifier: CA6399667
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2150622
ClinVar RCV Id: RCV003067662
dbSNP Id: rs765380398
ExAC: 12:5153915 G / T
gnomAD v2: 12-5153915-G-T
gnomAD v3: 12-5044749-G-T
gnomAD v4: 12-5044749-G-T
MyVariant Identifiers: chr12:g.5153915G>T (hg19) chr12:g.5044749G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044749G>T , CM000674.2:g.5044749G>T GRCh38
NC_000012.11:g.5153915G>T , CM000674.1:g.5153915G>T GRCh37
NC_000012.10:g.5024176G>T NCBI36
NG_012198.1:g.5831G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.602G>T MANE Select ENSP00000252321.3:p.Arg201Leu
ENST00000252321.4:c.602G>T ENSP00000252321.3:p.Arg201Leu
NM_002234.3:c.602G>T NP_002225.2:p.Arg201Leu
NM_002234.4:c.602G>T MANE Select NP_002225.2:p.Arg201Leu
Search 100 bp 5'
Search 100 bp 3'