Canonical Allele Identifier: CA6399936
Gene: KCNA5 HGNC NCBI

Linked Data

dbSNP Id: rs764006390
gnomAD v2: 12-5155048-G-A
gnomAD v4: 12-5045882-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5045882G>A , CM000674.2:g.5045882G>A GRCh38
NC_000012.11:g.5155048G>A , CM000674.1:g.5155048G>A GRCh37
NC_000012.10:g.5025309G>A NCBI36
NG_012198.1:g.6964G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252321.5:c.1735G>A MANE Select ENSP00000252321.3:p.Gly579Ser
ENST00000252321.4:c.1735G>A ENSP00000252321.3:p.Gly579Ser
NM_002234.3:c.1735G>A NP_002225.2:p.Gly579Ser
NM_002234.4:c.1735G>A MANE Select NP_002225.2:p.Gly579Ser