Canonical Allele Identifier: CA383454672
Gene: KCNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5021029G>C (hg19) chr12:g.4911863G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4911863G>C , CM000674.2:g.4911863G>C GRCh38
NC_000012.11:g.5021029G>C , CM000674.1:g.5021029G>C GRCh37
NC_000012.10:g.4891290G>C NCBI36
NG_011815.1:g.6957G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.485G>C MANE Select ENSP00000371985.3:p.Ser162Thr
ENST00000543874.3:n.105+1391G>C
ENST00000639306.1:c.323G>C ENSP00000492506.1:p.Ser108Thr
ENST00000382545.3:c.485G>C ENSP00000371985.3:p.Ser162Thr
ENST00000541095.1:n.105+1391G>C
ENST00000543874.2:n.96+1391G>C
NM_000217.2:c.485G>C NP_000208.2:p.Ser162Thr
NM_000217.3:c.485G>C MANE Select NP_000208.2:p.Ser162Thr
Search 100 bp 5'
Search 100 bp 3'