Canonical Allele Identifier: CA2374774349

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406984_63406985delinsCG , CM000682.2:g.63406984_63406985delinsCG	GRCh38
NC_000020.10:g.62038337_62038338delinsCG , CM000682.1:g.62038337_62038338delinsCG	GRCh37
NC_000020.9:g.61508781_61508782delinsCG	NCBI36
NG_009004.1:g.70656_70657delinsCG
NG_009004.2:g.70656_70657delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2332_2333delinsCG	ENSP00000516702.1:p.Arg778=
ENST00000359125.7:c.2278_2279delinsCG MANE Select	ENSP00000352035.2:p.Arg760=
ENST00000637193.1:c.1675_1676delinsCG	ENSP00000490734.1:p.Arg559=
ENST00000344462.8:c.2185_2186delinsCG	ENSP00000339611.4:p.Arg729=
ENST00000357249.6:c.1846_1847delinsCG	ENSP00000349789.3:p.Arg616=
ENST00000359125.6:c.2278_2279delinsCG	ENSP00000352035.2:p.Arg760=
ENST00000360480.7:c.2194_2195delinsCG	ENSP00000353668.3:p.Arg732=
ENST00000370224.5:c.2241+61_2241+62delinsCG	ENSP00000359244.2:n.2241+61_2241+62delinsCG
ENST00000625514.2:c.2205+61_2205+62delinsCG	ENSP00000486040.1:n.2205+61_2205+62delinsCG
ENST00000626839.2:c.2224_2225delinsCG	ENSP00000486706.1:p.Arg742=
ENST00000629241.2:c.2133+61_2133+62delinsCG	ENSP00000487142.1:n.2133+61_2133+62delinsCG
ENST00000629676.2:c.1680-6142_1680-6141delinsCG	ENSP00000486194.1:n.1680-6142_1680-6141delinsCG
NM_004518.4:c.2194_2195delinsCG	NP_004509.2:p.Arg732=
NM_172106.1:c.2224_2225delinsCG	NP_742104.1:p.Arg742=
NM_172107.2:c.2278_2279delinsCG	NP_742105.1:p.Arg760=
NM_172108.3:c.2185_2186delinsCG	NP_742106.1:p.Arg729=
XM_006723787.1:c.2320_2321delinsCG	XP_006723850.1:p.Arg774=
XM_011528807.1:c.2386_2387delinsCG	XP_011527109.1:p.Arg796=
XM_011528808.1:c.2383_2384delinsCG	XP_011527110.1:p.Arg795=
XM_011528809.1:c.2356_2357delinsCG	XP_011527111.1:p.Arg786=
XM_011528810.1:c.2332_2333delinsCG	XP_011527112.1:p.Arg778=
XM_011528811.1:c.2302_2303delinsCG	XP_011527113.1:p.Arg768=
XM_011528812.1:c.2275_2276delinsCG	XP_011527114.1:p.Arg759=
XM_011528813.1:c.2260_2261delinsCG	XP_011527115.1:p.Arg754=
XM_011528814.1:c.1867_1868delinsCG	XP_011527116.1:p.Arg623=
NM_004518.5:c.2194_2195delinsCG	NP_004509.2:p.Arg732=
NM_172106.2:c.2224_2225delinsCG	NP_742104.1:p.Arg742=
NM_172107.3:c.2278_2279delinsCG	NP_742105.1:p.Arg760=
NM_172108.4:c.2185_2186delinsCG	NP_742106.1:p.Arg729=
XM_011528810.2:c.2332_2333delinsCG	XP_011527112.1:p.Arg778=
XM_011528811.2:c.2302_2303delinsCG	XP_011527113.1:p.Arg768=
XM_017027841.2:c.2329_2330delinsCG	XP_016883330.1:p.Arg777=
XM_017027842.2:c.2266_2267delinsCG	XP_016883331.1:p.Arg756=
XM_017027843.1:c.2263_2264delinsCG	XP_016883332.1:p.Arg755=
XM_017027844.2:c.2221_2222delinsCG	XP_016883333.1:p.Arg741=
XM_017027845.1:c.1294_1295delinsCG	XP_016883334.1:p.Arg432=
NM_004518.6:c.2194_2195delinsCG	NP_004509.2:p.Arg732=
NM_172106.3:c.2224_2225delinsCG	NP_742104.1:p.Arg742=
NM_172107.4:c.2278_2279delinsCG MANE Select	NP_742105.1:p.Arg760=
NM_172108.5:c.2185_2186delinsCG	NP_742106.1:p.Arg729=
NM_001382235.1:c.2332_2333delinsCG	NP_001369164.1:p.Arg778=