Canonical Allele Identifier: CA2374787146

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63431398_63431399delinsGA , CM000682.2:g.63431398_63431399delinsGA	GRCh38
NC_000020.10:g.62062751_62062752delinsGA , CM000682.1:g.62062751_62062752delinsGA	GRCh37
NC_000020.9:g.61533195_61533196delinsGA	NCBI36
NG_009004.1:g.46242_46243delinsTC
NG_009004.2:g.46242_46243delinsTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1119-30_1119-29delinsTC	ENSP00000516702.1:n.1119-30_1119-29delinsTC
ENST00000359125.7:c.1119-30_1119-29delinsTC MANE Select	ENSP00000352035.2:n.1119-30_1119-29delinsTC
ENST00000636638.1:n.31+2047_31+2048delinsTC
ENST00000637193.1:c.599+2410_599+2411delinsTC	ENSP00000490734.1:n.599+2410_599+2411delinsTC
ENST00000344462.8:c.1119-30_1119-29delinsTC	ENSP00000339611.4:n.1119-30_1119-29delinsTC
ENST00000357249.6:c.777-30_777-29delinsTC	ENSP00000349789.3:n.777-30_777-29delinsTC
ENST00000359125.6:c.1119-30_1119-29delinsTC	ENSP00000352035.2:n.1119-30_1119-29delinsTC
ENST00000360480.7:c.1118+2410_1118+2411delinsTC	ENSP00000353668.3:n.1118+2410_1118+2411delinsTC
ENST00000370221.3:n.1245-30_1245-29delinsTC
ENST00000370224.5:c.1118+2410_1118+2411delinsTC	ENSP00000359244.2:n.1118+2410_1118+2411delinsTC
ENST00000625514.2:c.1118+2410_1118+2411delinsTC	ENSP00000486040.1:n.1118+2410_1118+2411delinsTC
ENST00000626839.2:c.1119-30_1119-29delinsTC	ENSP00000486706.1:n.1119-30_1119-29delinsTC
ENST00000627221.2:c.262+2410_262+2411delinsTC
ENST00000629241.2:c.1118+2410_1118+2411delinsTC	ENSP00000487142.1:n.1118+2410_1118+2411delinsTC
ENST00000629676.2:c.1118+2410_1118+2411delinsTC	ENSP00000486194.1:n.1118+2410_1118+2411delinsTC
NM_004518.4:c.1118+2410_1118+2411delinsTC	NP_004509.2:n.1118+2410_1118+2411delinsTC
NM_172106.1:c.1119-30_1119-29delinsTC	NP_742104.1:n.1119-30_1119-29delinsTC
NM_172107.2:c.1119-30_1119-29delinsTC	NP_742105.1:n.1119-30_1119-29delinsTC
NM_172108.3:c.1119-30_1119-29delinsTC	NP_742106.1:n.1119-30_1119-29delinsTC
XM_006723787.1:c.1119-30_1119-29delinsTC	XP_006723850.1:n.1119-30_1119-29delinsTC
XM_011528807.1:c.1119-30_1119-29delinsTC	XP_011527109.1:n.1119-30_1119-29delinsTC
XM_011528808.1:c.1119-30_1119-29delinsTC	XP_011527110.1:n.1119-30_1119-29delinsTC
XM_011528809.1:c.1118+2410_1118+2411delinsTC	XP_011527111.1:n.1118+2410_1118+2411delinsTC
XM_011528810.1:c.1119-30_1119-29delinsTC	XP_011527112.1:n.1119-30_1119-29delinsTC
XM_011528811.1:c.1118+2410_1118+2411delinsTC	XP_011527113.1:n.1118+2410_1118+2411delinsTC
XM_011528812.1:c.1119-30_1119-29delinsTC	XP_011527114.1:n.1119-30_1119-29delinsTC
XM_011528813.1:c.993-30_993-29delinsTC	XP_011527115.1:n.993-30_993-29delinsTC
XM_011528814.1:c.600-30_600-29delinsTC	XP_011527116.1:n.600-30_600-29delinsTC
XM_011528815.1:c.1119-30_1119-29delinsTC	XP_011527117.1:n.1119-30_1119-29delinsTC
NM_004518.5:c.1118+2410_1118+2411delinsTC	NP_004509.2:n.1118+2410_1118+2411delinsTC
NM_172106.2:c.1119-30_1119-29delinsTC	NP_742104.1:n.1119-30_1119-29delinsTC
NM_172107.3:c.1119-30_1119-29delinsTC	NP_742105.1:n.1119-30_1119-29delinsTC
NM_172108.4:c.1119-30_1119-29delinsTC	NP_742106.1:n.1119-30_1119-29delinsTC
XM_011528810.2:c.1119-30_1119-29delinsTC	XP_011527112.1:n.1119-30_1119-29delinsTC
XM_011528811.2:c.1118+2410_1118+2411delinsTC	XP_011527113.1:n.1118+2410_1118+2411delinsTC
XM_017027841.2:c.1119-30_1119-29delinsTC	XP_016883330.1:n.1119-30_1119-29delinsTC
XM_017027842.2:c.1119-30_1119-29delinsTC	XP_016883331.1:n.1119-30_1119-29delinsTC
XM_017027843.1:c.1050-30_1050-29delinsTC	XP_016883332.1:n.1050-30_1050-29delinsTC
XM_017027844.2:c.1119-30_1119-29delinsTC	XP_016883333.1:n.1119-30_1119-29delinsTC
NM_004518.6:c.1118+2410_1118+2411delinsTC	NP_004509.2:n.1118+2410_1118+2411delinsTC
NM_172106.3:c.1119-30_1119-29delinsTC	NP_742104.1:n.1119-30_1119-29delinsTC
NM_172107.4:c.1119-30_1119-29delinsTC MANE Select	NP_742105.1:n.1119-30_1119-29delinsTC
NM_172108.5:c.1119-30_1119-29delinsTC	NP_742106.1:n.1119-30_1119-29delinsTC
NM_001382235.1:c.1119-30_1119-29delinsTC	NP_001369164.1:n.1119-30_1119-29delinsTC