Canonical Allele Identifier: CA1140001514

Gene: KCNA2

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110605458C= , CM000663.2:g.110605458C=	GRCh38
NC_000001.10:g.111148080C= , CM000663.1:g.111148080C=	GRCh37
NC_000001.9:g.110949603C=	NCBI36
NG_027997.2:g.31017G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000316361.10:c.-231G= MANE Select	ENSP00000314520.4:n.-231G=
ENST00000485317.6:c.-231G=	ENSP00000433109.1:n.-231G=
ENST00000525120.2:n.294G=
ENST00000638477.2:c.-154G=	ENSP00000491354.1:n.-154G=
ENST00000638532.1:c.-231G=	ENSP00000491613.1:n.-231G=
ENST00000638616.2:c.-231G=	ENSP00000491977.1:n.-231G=
ENST00000639048.2:c.-154G=	ENSP00000491627.1:n.-154G=
ENST00000639233.2:c.-114G=	ENSP00000492716.1:n.-114G=
ENST00000640680.1:n.392G=
ENST00000640774.2:c.-154G=	ENSP00000492008.1:n.-154G=
ENST00000640956.1:c.-115G=	ENSP00000491647.1:n.-115G=
ENST00000675391.1:c.-441G=	ENSP00000502642.1:n.-441G=
ENST00000316361.8:c.-231G=	ENSP00000314520.4:n.-231G=
ENST00000369770.7:c.-231G=	ENSP00000358785.3:n.-231G=
ENST00000485317.5:c.-231G=	ENSP00000433109.1:n.-231G=
ENST00000525120.1:n.402G=
ENST00000633222.1:c.-231G=	ENSP00000487785.1:n.-231G=
NM_001204269.1:c.-231G=	NP_001191198.1:n.-231G=
NM_004974.3:c.-231G=	NP_004965.1:n.-231G=
XM_011541396.1:c.-231G=	XP_011539698.1:n.-231G=
XM_011541397.1:c.-231G=	XP_011539699.1:n.-231G=
XM_011541398.1:c.-231G=	XP_011539700.1:n.-231G=
XM_011541399.1:c.-231G=	XP_011539701.1:n.-231G=
XM_011541400.1:c.-231G=	XP_011539702.1:n.-231G=
XM_011541396.2:c.-231G=	XP_011539698.1:n.-231G=
XM_011541397.2:c.-231G=	XP_011539699.1:n.-231G=
XM_011541398.2:c.-231G=	XP_011539700.1:n.-231G=
XM_011541399.2:c.-231G=	XP_011539701.1:n.-231G=
XM_011541400.2:c.-231G=	XP_011539702.1:n.-231G=
XM_017001213.1:c.-231G=	XP_016856702.1:n.-231G=
NM_004974.4:c.-231G= MANE Select	NP_004965.1:n.-231G=
NM_001204269.2:c.-231G=	NP_001191198.1:n.-231G=