Canonical Allele Identifier: CA6399668
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2042557
ClinVar RCV Id: RCV002917569
dbSNP Id: rs758189575
ExAC: 12:5153925 G / A
gnomAD v2: 12-5153925-G-A
gnomAD v3: 12-5044759-G-A
gnomAD v4: 12-5044759-G-A
MyVariant Identifiers: chr12:g.5153925G>A (hg19) chr12:g.5044759G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044759G>A , CM000674.2:g.5044759G>A GRCh38
NC_000012.11:g.5153925G>A , CM000674.1:g.5153925G>A GRCh37
NC_000012.10:g.5024186G>A NCBI36
NG_012198.1:g.5841G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.612G>A MANE Select ENSP00000252321.3:p.Gln204=
ENST00000252321.4:c.612G>A ENSP00000252321.3:p.Gln204=
NM_002234.3:c.612G>A NP_002225.2:p.Gln204=
NM_002234.4:c.612G>A MANE Select NP_002225.2:p.Gln204=
Search 100 bp 5'
Search 100 bp 3'