Canonical Allele Identifier: CA478095169
Gene: KCNA5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5153976A>G (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.5044810A>G , CM000674.2:g.5044810A>G GRCh38
NC_000012.11:g.5153976A>G , CM000674.1:g.5153976A>G GRCh37
NC_000012.10:g.5024237A>G NCBI36
NG_012198.1:g.5892A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252321.5:c.663A>G MANE Select ENSP00000252321.3:p.Lys221=
ENST00000252321.4:c.663A>G ENSP00000252321.3:p.Lys221=
NM_002234.3:c.663A>G NP_002225.2:p.Lys221=
NM_002234.4:c.663A>G MANE Select NP_002225.2:p.Lys221=
Search 100 bp 5'
Search 100 bp 3'