Canonical Allele Identifier: CA478095030

Gene: KCNA1

Linked Data

• MyVariant Identifiers: chr12:g.5021786C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4912620C>T , CM000674.2:g.4912620C>T	GRCh38
NC_000012.11:g.5021786C>T , CM000674.1:g.5021786C>T	GRCh37
NC_000012.10:g.4892047C>T	NCBI36
NG_011815.1:g.7714C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382545.5:c.1242C>T MANE Select	ENSP00000371985.3:p.Phe414=
ENST00000543874.3:n.105+2148C>T
ENST00000639306.1:c.1080C>T	ENSP00000492506.1:p.Phe360=
ENST00000639680.1:c.76+354C>T
ENST00000382545.3:c.1242C>T	ENSP00000371985.3:p.Phe414=
ENST00000541095.1:n.105+2148C>T
ENST00000543874.2:n.96+2148C>T
NM_000217.2:c.1242C>T	NP_000208.2:p.Phe414=
NM_000217.3:c.1242C>T MANE Select	NP_000208.2:p.Phe414=