Canonical Allele Identifier: CA383454999
Gene: KCNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5021180C>A (hg19) chr12:g.4912014C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912014C>A , CM000674.2:g.4912014C>A GRCh38
NC_000012.11:g.5021180C>A , CM000674.1:g.5021180C>A GRCh37
NC_000012.10:g.4891441C>A NCBI36
NG_011815.1:g.7108C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.636C>A MANE Select ENSP00000371985.3:p.Tyr212Ter
ENST00000543874.3:n.105+1542C>A
ENST00000639306.1:c.474C>A ENSP00000492506.1:p.Tyr158Ter
ENST00000382545.3:c.636C>A ENSP00000371985.3:p.Tyr212Ter
ENST00000541095.1:n.105+1542C>A
ENST00000543874.2:n.96+1542C>A
NM_000217.2:c.636C>A NP_000208.2:p.Tyr212Ter
NM_000217.3:c.636C>A MANE Select NP_000208.2:p.Tyr212Ter
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