Canonical Allele Identifier: CA2374774332

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406952T= , CM000682.2:g.63406952T=	GRCh38
NC_000020.10:g.62038305T= , CM000682.1:g.62038305T=	GRCh37
NC_000020.9:g.61508749T=	NCBI36
NG_009004.1:g.70689A=
NG_009004.2:g.70689A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2365A=	ENSP00000516702.1:p.Thr789=
ENST00000359125.7:c.2311A= MANE Select	ENSP00000352035.2:p.Thr771=
ENST00000637193.1:c.1708A=	ENSP00000490734.1:p.Thr570=
ENST00000344462.8:c.2218A=	ENSP00000339611.4:p.Thr740=
ENST00000357249.6:c.1879A=	ENSP00000349789.3:p.Thr627=
ENST00000359125.6:c.2311A=	ENSP00000352035.2:p.Thr771=
ENST00000360480.7:c.2227A=	ENSP00000353668.3:p.Thr743=
ENST00000370224.5:c.2241+94A=	ENSP00000359244.2:n.2241+94A=
ENST00000625514.2:c.2205+94A=	ENSP00000486040.1:n.2205+94A=
ENST00000626839.2:c.2257A=	ENSP00000486706.1:p.Thr753=
ENST00000629241.2:c.2133+94A=	ENSP00000487142.1:n.2133+94A=
ENST00000629676.2:c.1680-6109A=	ENSP00000486194.1:n.1680-6109A=
NM_004518.4:c.2227A=	NP_004509.2:p.Thr743=
NM_172106.1:c.2257A=	NP_742104.1:p.Thr753=
NM_172107.2:c.2311A=	NP_742105.1:p.Thr771=
NM_172108.3:c.2218A=	NP_742106.1:p.Thr740=
XM_006723787.1:c.2353A=	XP_006723850.1:p.Thr785=
XM_011528807.1:c.2419A=	XP_011527109.1:p.Thr807=
XM_011528808.1:c.2416A=	XP_011527110.1:p.Thr806=
XM_011528809.1:c.2389A=	XP_011527111.1:p.Thr797=
XM_011528810.1:c.2365A=	XP_011527112.1:p.Thr789=
XM_011528811.1:c.2335A=	XP_011527113.1:p.Thr779=
XM_011528812.1:c.2308A=	XP_011527114.1:p.Thr770=
XM_011528813.1:c.2293A=	XP_011527115.1:p.Thr765=
XM_011528814.1:c.1900A=	XP_011527116.1:p.Thr634=
NM_004518.5:c.2227A=	NP_004509.2:p.Thr743=
NM_172106.2:c.2257A=	NP_742104.1:p.Thr753=
NM_172107.3:c.2311A=	NP_742105.1:p.Thr771=
NM_172108.4:c.2218A=	NP_742106.1:p.Thr740=
XM_011528810.2:c.2365A=	XP_011527112.1:p.Thr789=
XM_011528811.2:c.2335A=	XP_011527113.1:p.Thr779=
XM_017027841.2:c.2362A=	XP_016883330.1:p.Thr788=
XM_017027842.2:c.2299A=	XP_016883331.1:p.Thr767=
XM_017027843.1:c.2296A=	XP_016883332.1:p.Thr766=
XM_017027844.2:c.2254A=	XP_016883333.1:p.Thr752=
XM_017027845.1:c.1327A=	XP_016883334.1:p.Thr443=
NM_004518.6:c.2227A=	NP_004509.2:p.Thr743=
NM_172106.3:c.2257A=	NP_742104.1:p.Thr753=
NM_172107.4:c.2311A= MANE Select	NP_742105.1:p.Thr771=
NM_172108.5:c.2218A=	NP_742106.1:p.Thr740=
NM_001382235.1:c.2365A=	NP_001369164.1:p.Thr789=