Canonical Allele Identifier: CA478095602
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs1400673691
gnomAD v3: 12-5045353-C-A
gnomAD v4: 12-5045353-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045353C>A , CM000674.2:g.5045353C>A GRCh38
NC_000012.11:g.5154519C>A , CM000674.1:g.5154519C>A GRCh37
NC_000012.10:g.5024780C>A NCBI36
NG_012198.1:g.6435C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.1206C>A MANE Select ENSP00000252321.3:p.Ile402=
ENST00000252321.4:c.1206C>A ENSP00000252321.3:p.Ile402=
NM_002234.3:c.1206C>A NP_002225.2:p.Ile402=
NM_002234.4:c.1206C>A MANE Select NP_002225.2:p.Ile402=