Canonical Allele Identifier: CA383454727
Gene: KCNA1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.5021056T>G (hg19) chr12:g.4911890T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.4911890T>G , CM000674.2:g.4911890T>G GRCh38
NC_000012.11:g.5021056T>G , CM000674.1:g.5021056T>G GRCh37
NC_000012.10:g.4891317T>G NCBI36
NG_011815.1:g.6984T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000382545.5:c.512T>G MANE Select ENSP00000371985.3:p.Ile171Ser
ENST00000543874.3:n.105+1418T>G
ENST00000639306.1:c.350T>G ENSP00000492506.1:p.Ile117Ser
ENST00000382545.3:c.512T>G ENSP00000371985.3:p.Ile171Ser
ENST00000541095.1:n.105+1418T>G
ENST00000543874.2:n.96+1418T>G
NM_000217.2:c.512T>G NP_000208.2:p.Ile171Ser
NM_000217.3:c.512T>G MANE Select NP_000208.2:p.Ile171Ser
Search 100 bp 5'
Search 100 bp 3'