Canonical Allele Identifier: CA478095904
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1862773332
gnomAD v3: 12-5045890-C-T
gnomAD v4: 12-5045890-C-T
MyVariant Identifiers: chr12:g.5155056C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045890C>T , CM000674.2:g.5045890C>T GRCh38
NC_000012.11:g.5155056C>T , CM000674.1:g.5155056C>T GRCh37
NC_000012.10:g.5025317C>T NCBI36
NG_012198.1:g.6972C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1743C>T MANE Select ENSP00000252321.3:p.Cys581=
ENST00000252321.4:c.1743C>T ENSP00000252321.3:p.Cys581=
NM_002234.3:c.1743C>T NP_002225.2:p.Cys581=
NM_002234.4:c.1743C>T MANE Select NP_002225.2:p.Cys581=