Canonical Allele Identifier: CA2374774279

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406865G= , CM000682.2:g.63406865G=	GRCh38
NC_000020.10:g.62038218G= , CM000682.1:g.62038218G=	GRCh37
NC_000020.9:g.61508662G=	NCBI36
NG_009004.1:g.70776C=
NG_009004.2:g.70776C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2452C=	ENSP00000516702.1:p.Arg818=
ENST00000359125.7:c.2398C= MANE Select	ENSP00000352035.2:p.Arg800=
ENST00000637193.1:c.1795C=	ENSP00000490734.1:p.Arg599=
ENST00000344462.8:c.2305C=	ENSP00000339611.4:p.Arg769=
ENST00000357249.6:c.1966C=	ENSP00000349789.3:p.Arg656=
ENST00000359125.6:c.2398C=	ENSP00000352035.2:p.Arg800=
ENST00000360480.7:c.2314C=	ENSP00000353668.3:p.Arg772=
ENST00000370224.5:c.2241+181C=	ENSP00000359244.2:n.2241+181C=
ENST00000625514.2:c.2205+181C=	ENSP00000486040.1:n.2205+181C=
ENST00000626839.2:c.2344C=	ENSP00000486706.1:p.Arg782=
ENST00000629241.2:c.2133+181C=	ENSP00000487142.1:n.2133+181C=
ENST00000629676.2:c.1680-6022C=	ENSP00000486194.1:n.1680-6022C=
NM_004518.4:c.2314C=	NP_004509.2:p.Arg772=
NM_172106.1:c.2344C=	NP_742104.1:p.Arg782=
NM_172107.2:c.2398C=	NP_742105.1:p.Arg800=
NM_172108.3:c.2305C=	NP_742106.1:p.Arg769=
XM_006723787.1:c.2440C=	XP_006723850.1:p.Arg814=
XM_011528807.1:c.2506C=	XP_011527109.1:p.Arg836=
XM_011528808.1:c.2503C=	XP_011527110.1:p.Arg835=
XM_011528809.1:c.2476C=	XP_011527111.1:p.Arg826=
XM_011528810.1:c.2452C=	XP_011527112.1:p.Arg818=
XM_011528811.1:c.2422C=	XP_011527113.1:p.Arg808=
XM_011528812.1:c.2395C=	XP_011527114.1:p.Arg799=
XM_011528813.1:c.2380C=	XP_011527115.1:p.Arg794=
XM_011528814.1:c.1987C=	XP_011527116.1:p.Arg663=
NM_004518.5:c.2314C=	NP_004509.2:p.Arg772=
NM_172106.2:c.2344C=	NP_742104.1:p.Arg782=
NM_172107.3:c.2398C=	NP_742105.1:p.Arg800=
NM_172108.4:c.2305C=	NP_742106.1:p.Arg769=
XM_011528810.2:c.2452C=	XP_011527112.1:p.Arg818=
XM_011528811.2:c.2422C=	XP_011527113.1:p.Arg808=
XM_017027841.2:c.2449C=	XP_016883330.1:p.Arg817=
XM_017027842.2:c.2386C=	XP_016883331.1:p.Arg796=
XM_017027843.1:c.2383C=	XP_016883332.1:p.Arg795=
XM_017027844.2:c.2341C=	XP_016883333.1:p.Arg781=
XM_017027845.1:c.1414C=	XP_016883334.1:p.Arg472=
NM_004518.6:c.2314C=	NP_004509.2:p.Arg772=
NM_172106.3:c.2344C=	NP_742104.1:p.Arg782=
NM_172107.4:c.2398C= MANE Select	NP_742105.1:p.Arg800=
NM_172108.5:c.2305C=	NP_742106.1:p.Arg769=
NM_001382235.1:c.2452C=	NP_001369164.1:p.Arg818=