Canonical Allele Identifier: CA383466161

Gene: KCNA5

Linked Data

• MyVariant Identifiers: chr12:g.5154602C>A (hg19) ; chr12:g.5045436C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.5045436C>A , CM000674.2:g.5045436C>A	GRCh38
NC_000012.11:g.5154602C>A , CM000674.1:g.5154602C>A	GRCh37
NC_000012.10:g.5024863C>A	NCBI36
NG_012198.1:g.6518C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252321.5:c.1289C>A MANE Select	ENSP00000252321.3:p.Ser430Tyr
ENST00000252321.4:c.1289C>A	ENSP00000252321.3:p.Ser430Tyr
NM_002234.3:c.1289C>A	NP_002225.2:p.Ser430Tyr
NM_002234.4:c.1289C>A MANE Select	NP_002225.2:p.Ser430Tyr