Canonical Allele Identifier: CA1188577445

Gene: KCNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110603794A= , CM000663.2:g.110603794A=	GRCh38
NC_000001.10:g.111146416A= , CM000663.1:g.111146416A=	GRCh37
NC_000001.9:g.110947939A=	NCBI36
NG_027997.2:g.32681T=

Transcript Alleles

HGVS	Amino-acid Change
NM_004974.4:c.989T= MANE Select	NP_004965.1:p.Leu330=
ENST00000316361.10:c.989T= MANE Select	ENSP00000314520.4:p.Leu330=
NM_001204269.1:c.894+95T=	NP_001191198.1:n.894+95T=
NM_001204269.2:c.894+95T=	NP_001191198.1:n.894+95T=
NM_004974.3:c.989T=	NP_004965.1:p.Leu330=
ENST00000316361.8:c.989T=	ENSP00000314520.4:p.Leu330=
ENST00000369770.7:c.894+95T=	ENSP00000358785.3:n.894+95T=
ENST00000485317.5:c.989T=	ENSP00000433109.1:p.Leu330=
ENST00000485317.6:c.989T=	ENSP00000433109.1:p.Leu330=
ENST00000525120.2:n.361+1597T=
ENST00000633222.1:c.989T=	ENSP00000487785.1:p.Leu330=
ENST00000638477.2:c.128+99T=	ENSP00000491354.1:n.128+99T=
ENST00000638532.1:c.989T=	ENSP00000491613.1:p.Leu330=
ENST00000638616.2:c.989T=	ENSP00000491977.1:p.Leu330=
ENST00000639048.2:c.227T=	ENSP00000491627.1:p.Leu76=
ENST00000639227.1:n.658+99T=
ENST00000639233.2:c.407T=	ENSP00000492716.1:p.Leu136=
ENST00000640450.1:n.998+99T=
ENST00000640680.1:n.459+1597T=
ENST00000640774.2:c.132+95T=	ENSP00000492008.1:n.132+95T=
ENST00000640956.1:c.623T=	ENSP00000491647.1:p.Leu208=
ENST00000675391.1:c.989T=	ENSP00000502642.1:p.Leu330=
XM_011541396.1:c.989T=	XP_011539698.1:p.Leu330=
XM_011541396.2:c.989T=	XP_011539698.1:p.Leu330=
XM_011541397.1:c.989T=	XP_011539699.1:p.Leu330=
XM_011541397.2:c.989T=	XP_011539699.1:p.Leu330=
XM_011541398.1:c.989T=	XP_011539700.1:p.Leu330=
XM_011541398.2:c.989T=	XP_011539700.1:p.Leu330=
XM_011541399.1:c.989T=	XP_011539701.1:p.Leu330=
XM_011541399.2:c.989T=	XP_011539701.1:p.Leu330=
XM_011541400.1:c.989T=	XP_011539702.1:p.Leu330=
XM_011541400.2:c.989T=	XP_011539702.1:p.Leu330=
XM_017001213.1:c.989T=	XP_016856702.1:p.Leu330=