Canonical Allele Identifier: CA478094183
Gene: KCNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5021030C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4911864C>T , CM000674.2:g.4911864C>T GRCh38
NC_000012.11:g.5021030C>T , CM000674.1:g.5021030C>T GRCh37
NC_000012.10:g.4891291C>T NCBI36
NG_011815.1:g.6958C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.486C>T MANE Select ENSP00000371985.3:p.Ser162=
ENST00000543874.3:n.105+1392C>T
ENST00000639306.1:c.324C>T ENSP00000492506.1:p.Ser108=
ENST00000382545.3:c.486C>T ENSP00000371985.3:p.Ser162=
ENST00000541095.1:n.105+1392C>T
ENST00000543874.2:n.96+1392C>T
NM_000217.2:c.486C>T NP_000208.2:p.Ser162=
NM_000217.3:c.486C>T MANE Select NP_000208.2:p.Ser162=