Canonical Allele Identifier: CA478095002

Gene: KCNA1

Linked Data

• MyVariant Identifiers: chr12:g.5021768G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.4912602G>T , CM000674.2:g.4912602G>T	GRCh38
NC_000012.11:g.5021768G>T , CM000674.1:g.5021768G>T	GRCh37
NC_000012.10:g.4892029G>T	NCBI36
NG_011815.1:g.7696G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000382545.5:c.1224G>T MANE Select	ENSP00000371985.3:p.Val408=
ENST00000543874.3:n.105+2130G>T
ENST00000639306.1:c.1062G>T	ENSP00000492506.1:p.Val354=
ENST00000639680.1:c.76+336G>T
ENST00000382545.3:c.1224G>T	ENSP00000371985.3:p.Val408=
ENST00000541095.1:n.105+2130G>T
ENST00000543874.2:n.96+2130G>T
NM_000217.2:c.1224G>T	NP_000208.2:p.Val408=
NM_000217.3:c.1224G>T MANE Select	NP_000208.2:p.Val408=