Canonical Allele Identifier: CA6399884
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 701419
ClinVar RCV Id: RCV000869954
dbSNP Id: rs748151274
ExAC: 12:5154822 C / T
gnomAD v2: 12-5154822-C-T
gnomAD v3: 12-5045656-C-T
gnomAD v4: 12-5045656-C-T
COSMIC: COSM4629962
MyVariant Identifiers: chr12:g.5154822C>T (hg19) chr12:g.5154822_5154823delinsTG (hg19) chr12:g.5045656C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045656C>T , CM000674.2:g.5045656C>T GRCh38
NC_000012.11:g.5154822C>T , CM000674.1:g.5154822C>T GRCh37
NC_000012.10:g.5025083C>T NCBI36
NG_012198.1:g.6738C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1509C>T MANE Select ENSP00000252321.3:p.Ala503=
ENST00000252321.4:c.1509C>T ENSP00000252321.3:p.Ala503=
NM_002234.3:c.1509C>T NP_002225.2:p.Ala503=
NM_002234.4:c.1509C>T MANE Select NP_002225.2:p.Ala503=
Search 100 bp 5'
Search 100 bp 3'