Canonical Allele Identifier: CA383456092
Gene: KCNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5021667T>C (hg19) chr12:g.4912501T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4912501T>C , CM000674.2:g.4912501T>C GRCh38
NC_000012.11:g.5021667T>C , CM000674.1:g.5021667T>C GRCh37
NC_000012.10:g.4891928T>C NCBI36
NG_011815.1:g.7595T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000382545.5:c.1123T>C MANE Select ENSP00000371985.3:p.Tyr375His
ENST00000543874.3:n.105+2029T>C
ENST00000639306.1:c.961T>C ENSP00000492506.1:p.Tyr321His
ENST00000639680.1:c.76+235T>C
ENST00000382545.3:c.1123T>C ENSP00000371985.3:p.Tyr375His
ENST00000541095.1:n.105+2029T>C
ENST00000543874.2:n.96+2029T>C
NM_000217.2:c.1123T>C NP_000208.2:p.Tyr375His
NM_000217.3:c.1123T>C MANE Select NP_000208.2:p.Tyr375His
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