Canonical Allele Identifier: CA6399911
Gene: KCNA5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1023092
ClinVar RCV Id: RCV001323090
dbSNP Id: rs142289285
gnomAD v2: 12-5154949-C-T
gnomAD v3: 12-5045783-C-T
gnomAD v4: 12-5045783-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045783C>T , CM000674.2:g.5045783C>T GRCh38
NC_000012.11:g.5154949C>T , CM000674.1:g.5154949C>T GRCh37
NC_000012.10:g.5025210C>T NCBI36
NG_012198.1:g.6865C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1636C>T MANE Select ENSP00000252321.3:p.Pro546Ser
ENST00000252321.4:c.1636C>T ENSP00000252321.3:p.Pro546Ser
NM_002234.3:c.1636C>T NP_002225.2:p.Pro546Ser
NM_002234.4:c.1636C>T MANE Select NP_002225.2:p.Pro546Ser