Canonical Allele Identifier: CA478094982

Gene: KCNA1

Linked Data

• MyVariant Identifiers: chr12:g.5021759T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4912593T>C , CM000674.2:g.4912593T>C	GRCh38
NC_000012.11:g.5021759T>C , CM000674.1:g.5021759T>C	GRCh37
NC_000012.10:g.4892020T>C	NCBI36
NG_011815.1:g.7687T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382545.5:c.1215T>C MANE Select	ENSP00000371985.3:p.Pro405=
ENST00000543874.3:n.105+2121T>C
ENST00000639306.1:c.1053T>C	ENSP00000492506.1:p.Pro351=
ENST00000639680.1:c.76+327T>C
ENST00000382545.3:c.1215T>C	ENSP00000371985.3:p.Pro405=
ENST00000541095.1:n.105+2121T>C
ENST00000543874.2:n.96+2121T>C
NM_000217.2:c.1215T>C	NP_000208.2:p.Pro405=
NM_000217.3:c.1215T>C MANE Select	NP_000208.2:p.Pro405=