Canonical Allele Identifier: CA383462053
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1402989
ClinVar RCV Id: RCV001897096
dbSNP Id: rs1383675030
gnomAD v2: 12-5153492-C-G
gnomAD v3: 12-5044326-C-G
gnomAD v4: 12-5044326-C-G
MyVariant Identifiers: chr12:g.5153492C>G (hg19) chr12:g.5044326C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044326C>G , CM000674.2:g.5044326C>G GRCh38
NC_000012.11:g.5153492C>G , CM000674.1:g.5153492C>G GRCh37
NC_000012.10:g.5023753C>G NCBI36
NG_012198.1:g.5408C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.179C>G MANE Select ENSP00000252321.3:p.Ala60Gly
ENST00000252321.4:c.179C>G ENSP00000252321.3:p.Ala60Gly
NM_002234.3:c.179C>G NP_002225.2:p.Ala60Gly
NM_002234.4:c.179C>G MANE Select NP_002225.2:p.Ala60Gly
Search 100 bp 5'
Search 100 bp 3'