Canonical Allele Identifier: CA478094928

Gene: KCNA1

Linked Data

• MyVariant Identifiers: chr12:g.5021732T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4912566T>G , CM000674.2:g.4912566T>G	GRCh38
NC_000012.11:g.5021732T>G , CM000674.1:g.5021732T>G	GRCh37
NC_000012.10:g.4891993T>G	NCBI36
NG_011815.1:g.7660T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382545.5:c.1188T>G MANE Select	ENSP00000371985.3:p.Gly396=
ENST00000543874.3:n.105+2094T>G
ENST00000639306.1:c.1026T>G	ENSP00000492506.1:p.Gly342=
ENST00000639680.1:c.76+300T>G
ENST00000382545.3:c.1188T>G	ENSP00000371985.3:p.Gly396=
ENST00000541095.1:n.105+2094T>G
ENST00000543874.2:n.96+2094T>G
NM_000217.2:c.1188T>G	NP_000208.2:p.Gly396=
NM_000217.3:c.1188T>G MANE Select	NP_000208.2:p.Gly396=