Canonical Allele Identifier: CA1188577468

Gene: KCNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110603893C= , CM000663.2:g.110603893C=	GRCh38
NC_000001.10:g.111146515C= , CM000663.1:g.111146515C=	GRCh37
NC_000001.9:g.110948038C=	NCBI36
NG_027997.2:g.32582G=

Transcript Alleles

HGVS	Amino-acid Change
NM_004974.4:c.890G= MANE Select	NP_004965.1:p.Arg297=
ENST00000316361.10:c.890G= MANE Select	ENSP00000314520.4:p.Arg297=
NM_001204269.1:c.890G=	NP_001191198.1:p.Arg297=
NM_001204269.2:c.890G=	NP_001191198.1:p.Arg297=
NM_004974.3:c.890G=	NP_004965.1:p.Arg297=
ENST00000316361.8:c.890G=	ENSP00000314520.4:p.Arg297=
ENST00000369770.7:c.890G=	ENSP00000358785.3:p.Arg297=
ENST00000485317.5:c.890G=	ENSP00000433109.1:p.Arg297=
ENST00000485317.6:c.890G=	ENSP00000433109.1:p.Arg297=
ENST00000525120.2:n.361+1498G=
ENST00000633222.1:c.890G=	ENSP00000487785.1:p.Arg297=
ENST00000638477.2:c.128G=	ENSP00000491354.1:p.Arg43=
ENST00000638532.1:c.890G=	ENSP00000491613.1:p.Arg297=
ENST00000638616.2:c.890G=	ENSP00000491977.1:p.Arg297=
ENST00000639048.2:c.128G=	ENSP00000491627.1:p.Arg43=
ENST00000639227.1:n.658G=
ENST00000639233.2:c.308G=	ENSP00000492716.1:p.Arg103=
ENST00000640450.1:n.998G=
ENST00000640680.1:n.459+1498G=
ENST00000640774.2:c.128G=	ENSP00000492008.1:p.Arg43=
ENST00000640956.1:c.524G=	ENSP00000491647.1:p.Arg175=
ENST00000675391.1:c.890G=	ENSP00000502642.1:p.Arg297=
XM_011541396.1:c.890G=	XP_011539698.1:p.Arg297=
XM_011541396.2:c.890G=	XP_011539698.1:p.Arg297=
XM_011541397.1:c.890G=	XP_011539699.1:p.Arg297=
XM_011541397.2:c.890G=	XP_011539699.1:p.Arg297=
XM_011541398.1:c.890G=	XP_011539700.1:p.Arg297=
XM_011541398.2:c.890G=	XP_011539700.1:p.Arg297=
XM_011541399.1:c.890G=	XP_011539701.1:p.Arg297=
XM_011541399.2:c.890G=	XP_011539701.1:p.Arg297=
XM_011541400.1:c.890G=	XP_011539702.1:p.Arg297=
XM_011541400.2:c.890G=	XP_011539702.1:p.Arg297=
XM_017001213.1:c.890G=	XP_016856702.1:p.Arg297=