Canonical Allele Identifier: CA2374774318

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406935_63406937delinsGGG , CM000682.2:g.63406935_63406937delinsGGG	GRCh38
NC_000020.10:g.62038288_62038290delinsGGG , CM000682.1:g.62038288_62038290delinsGGG	GRCh37
NC_000020.9:g.61508732_61508734delinsGGG	NCBI36
NG_009004.1:g.70704_70706delinsCCC
NG_009004.2:g.70704_70706delinsCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2380_2382delinsCCC	ENSP00000516702.1:p.Pro794=
ENST00000359125.7:c.2326_2328delinsCCC MANE Select	ENSP00000352035.2:p.Pro776=
ENST00000637193.1:c.1723_1725delinsCCC	ENSP00000490734.1:p.Pro575=
ENST00000344462.8:c.2233_2235delinsCCC	ENSP00000339611.4:p.Pro745=
ENST00000357249.6:c.1894_1896delinsCCC	ENSP00000349789.3:p.Pro632=
ENST00000359125.6:c.2326_2328delinsCCC	ENSP00000352035.2:p.Pro776=
ENST00000360480.7:c.2242_2244delinsCCC	ENSP00000353668.3:p.Pro748=
ENST00000370224.5:c.2241+109_2241+111delinsCCC	ENSP00000359244.2:n.2241+109_2241+111delinsCCC
ENST00000625514.2:c.2205+109_2205+111delinsCCC	ENSP00000486040.1:n.2205+109_2205+111delinsCCC
ENST00000626839.2:c.2272_2274delinsCCC	ENSP00000486706.1:p.Pro758=
ENST00000629241.2:c.2133+109_2133+111delinsCCC	ENSP00000487142.1:n.2133+109_2133+111delinsCCC
ENST00000629676.2:c.1680-6094_1680-6092delinsCCC	ENSP00000486194.1:n.1680-6094_1680-6092delinsCCC
NM_004518.4:c.2242_2244delinsCCC	NP_004509.2:p.Pro748=
NM_172106.1:c.2272_2274delinsCCC	NP_742104.1:p.Pro758=
NM_172107.2:c.2326_2328delinsCCC	NP_742105.1:p.Pro776=
NM_172108.3:c.2233_2235delinsCCC	NP_742106.1:p.Pro745=
XM_006723787.1:c.2368_2370delinsCCC	XP_006723850.1:p.Pro790=
XM_011528807.1:c.2434_2436delinsCCC	XP_011527109.1:p.Pro812=
XM_011528808.1:c.2431_2433delinsCCC	XP_011527110.1:p.Pro811=
XM_011528809.1:c.2404_2406delinsCCC	XP_011527111.1:p.Pro802=
XM_011528810.1:c.2380_2382delinsCCC	XP_011527112.1:p.Pro794=
XM_011528811.1:c.2350_2352delinsCCC	XP_011527113.1:p.Pro784=
XM_011528812.1:c.2323_2325delinsCCC	XP_011527114.1:p.Pro775=
XM_011528813.1:c.2308_2310delinsCCC	XP_011527115.1:p.Pro770=
XM_011528814.1:c.1915_1917delinsCCC	XP_011527116.1:p.Pro639=
NM_004518.5:c.2242_2244delinsCCC	NP_004509.2:p.Pro748=
NM_172106.2:c.2272_2274delinsCCC	NP_742104.1:p.Pro758=
NM_172107.3:c.2326_2328delinsCCC	NP_742105.1:p.Pro776=
NM_172108.4:c.2233_2235delinsCCC	NP_742106.1:p.Pro745=
XM_011528810.2:c.2380_2382delinsCCC	XP_011527112.1:p.Pro794=
XM_011528811.2:c.2350_2352delinsCCC	XP_011527113.1:p.Pro784=
XM_017027841.2:c.2377_2379delinsCCC	XP_016883330.1:p.Pro793=
XM_017027842.2:c.2314_2316delinsCCC	XP_016883331.1:p.Pro772=
XM_017027843.1:c.2311_2313delinsCCC	XP_016883332.1:p.Pro771=
XM_017027844.2:c.2269_2271delinsCCC	XP_016883333.1:p.Pro757=
XM_017027845.1:c.1342_1344delinsCCC	XP_016883334.1:p.Pro448=
NM_004518.6:c.2242_2244delinsCCC	NP_004509.2:p.Pro748=
NM_172106.3:c.2272_2274delinsCCC	NP_742104.1:p.Pro758=
NM_172107.4:c.2326_2328delinsCCC MANE Select	NP_742105.1:p.Pro776=
NM_172108.5:c.2233_2235delinsCCC	NP_742106.1:p.Pro745=
NM_001382235.1:c.2380_2382delinsCCC	NP_001369164.1:p.Pro794=