Canonical Allele Identifier: CA383455061

Gene: KCNA1

Linked Data

• MyVariant Identifiers: chr12:g.5021208T>C (hg19) ; chr12:g.4912042T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4912042T>C , CM000674.2:g.4912042T>C	GRCh38
NC_000012.11:g.5021208T>C , CM000674.1:g.5021208T>C	GRCh37
NC_000012.10:g.4891469T>C	NCBI36
NG_011815.1:g.7136T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382545.5:c.664T>C MANE Select	ENSP00000371985.3:p.Phe222Leu
ENST00000543874.3:n.105+1570T>C
ENST00000639306.1:c.502T>C	ENSP00000492506.1:p.Phe168Leu
ENST00000382545.3:c.664T>C	ENSP00000371985.3:p.Phe222Leu
ENST00000541095.1:n.105+1570T>C
ENST00000543874.2:n.96+1570T>C
NM_000217.2:c.664T>C	NP_000208.2:p.Phe222Leu
NM_000217.3:c.664T>C MANE Select	NP_000208.2:p.Phe222Leu