Canonical Allele Identifier: CA383467010

Gene: KCNA5

Linked Data

• dbSNP Id: rs1375359685
• gnomAD v2: 12-5155000-T-A
• gnomAD v4: 12-5045834-T-A
• MyVariant Identifiers: chr12:g.5155000T>A (hg19) ; chr12:g.5045834T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.5045834T>A , CM000674.2:g.5045834T>A	GRCh38
NC_000012.11:g.5155000T>A , CM000674.1:g.5155000T>A	GRCh37
NC_000012.10:g.5025261T>A	NCBI36
NG_012198.1:g.6916T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252321.5:c.1687T>A MANE Select	ENSP00000252321.3:p.Phe563Ile
ENST00000252321.4:c.1687T>A	ENSP00000252321.3:p.Phe563Ile
NM_002234.3:c.1687T>A	NP_002225.2:p.Phe563Ile
NM_002234.4:c.1687T>A MANE Select	NP_002225.2:p.Phe563Ile