Canonical Allele Identifier: CA478094843
Gene: KCNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5021684T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912518T>G , CM000674.2:g.4912518T>G GRCh38
NC_000012.11:g.5021684T>G , CM000674.1:g.5021684T>G GRCh37
NC_000012.10:g.4891945T>G NCBI36
NG_011815.1:g.7612T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.1140T>G MANE Select ENSP00000371985.3:p.Pro380=
ENST00000543874.3:n.105+2046T>G
ENST00000639306.1:c.978T>G ENSP00000492506.1:p.Pro326=
ENST00000639680.1:c.76+252T>G
ENST00000382545.3:c.1140T>G ENSP00000371985.3:p.Pro380=
ENST00000541095.1:n.105+2046T>G
ENST00000543874.2:n.96+2046T>G
NM_000217.2:c.1140T>G NP_000208.2:p.Pro380=
NM_000217.3:c.1140T>G MANE Select NP_000208.2:p.Pro380=