Canonical Allele Identifier: CA383455653

Gene: KCNA1

Linked Data

• ClinVar Variation Id: 3236197
• ClinVar RCV Id: RCV004555453
• MyVariant Identifiers: chr12:g.5021474G>C (hg19) ; chr12:g.4912308G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4912308G>C , CM000674.2:g.4912308G>C	GRCh38
NC_000012.11:g.5021474G>C , CM000674.1:g.5021474G>C	GRCh37
NC_000012.10:g.4891735G>C	NCBI36
NG_011815.1:g.7402G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382545.5:c.930G>C MANE Select	ENSP00000371985.3:p.Lys310Asn
ENST00000543874.3:n.105+1836G>C
ENST00000639306.1:c.768G>C	ENSP00000492506.1:p.Lys256Asn
ENST00000639680.1:c.76+42G>C
ENST00000382545.3:c.930G>C	ENSP00000371985.3:p.Lys310Asn
ENST00000541095.1:n.105+1836G>C
ENST00000543874.2:n.96+1836G>C
NM_000217.2:c.930G>C	NP_000208.2:p.Lys310Asn
NM_000217.3:c.930G>C MANE Select	NP_000208.2:p.Lys310Asn