Canonical Allele Identifier: CA2374774368
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407015G= , CM000682.2:g.63407015G= GRCh38
NC_000020.10:g.62038368G= , CM000682.1:g.62038368G= GRCh37
NC_000020.9:g.61508812G= NCBI36
NG_009004.1:g.70626C=
NG_009004.2:g.70626C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2302C= ENSP00000516702.1:p.Arg768=
ENST00000359125.7:c.2248C= MANE Select ENSP00000352035.2:p.Arg750=
ENST00000637193.1:c.1645C= ENSP00000490734.1:p.Arg549=
ENST00000344462.8:c.2155C= ENSP00000339611.4:p.Arg719=
ENST00000357249.6:c.1816C= ENSP00000349789.3:p.Arg606=
ENST00000359125.6:c.2248C= ENSP00000352035.2:p.Arg750=
ENST00000360480.7:c.2164C= ENSP00000353668.3:p.Arg722=
ENST00000370224.5:c.2241+31C= ENSP00000359244.2:n.2241+31C=
ENST00000625514.2:c.2205+31C= ENSP00000486040.1:n.2205+31C=
ENST00000626839.2:c.2194C= ENSP00000486706.1:p.Arg732=
ENST00000629241.2:c.2133+31C= ENSP00000487142.1:n.2133+31C=
ENST00000629676.2:c.1680-6172C= ENSP00000486194.1:n.1680-6172C=
NM_004518.4:c.2164C= NP_004509.2:p.Arg722=
NM_172106.1:c.2194C= NP_742104.1:p.Arg732=
NM_172107.2:c.2248C= NP_742105.1:p.Arg750=
NM_172108.3:c.2155C= NP_742106.1:p.Arg719=
XM_006723787.1:c.2290C= XP_006723850.1:p.Arg764=
XM_011528807.1:c.2356C= XP_011527109.1:p.Arg786=
XM_011528808.1:c.2353C= XP_011527110.1:p.Arg785=
XM_011528809.1:c.2326C= XP_011527111.1:p.Arg776=
XM_011528810.1:c.2302C= XP_011527112.1:p.Arg768=
XM_011528811.1:c.2272C= XP_011527113.1:p.Arg758=
XM_011528812.1:c.2245C= XP_011527114.1:p.Arg749=
XM_011528813.1:c.2230C= XP_011527115.1:p.Arg744=
XM_011528814.1:c.1837C= XP_011527116.1:p.Arg613=
NM_004518.5:c.2164C= NP_004509.2:p.Arg722=
NM_172106.2:c.2194C= NP_742104.1:p.Arg732=
NM_172107.3:c.2248C= NP_742105.1:p.Arg750=
NM_172108.4:c.2155C= NP_742106.1:p.Arg719=
XM_011528810.2:c.2302C= XP_011527112.1:p.Arg768=
XM_011528811.2:c.2272C= XP_011527113.1:p.Arg758=
XM_017027841.2:c.2299C= XP_016883330.1:p.Arg767=
XM_017027842.2:c.2236C= XP_016883331.1:p.Arg746=
XM_017027843.1:c.2233C= XP_016883332.1:p.Arg745=
XM_017027844.2:c.2191C= XP_016883333.1:p.Arg731=
XM_017027845.1:c.1264C= XP_016883334.1:p.Arg422=
NM_004518.6:c.2164C= NP_004509.2:p.Arg722=
NM_172106.3:c.2194C= NP_742104.1:p.Arg732=
NM_172107.4:c.2248C= MANE Select NP_742105.1:p.Arg750=
NM_172108.5:c.2155C= NP_742106.1:p.Arg719=
NM_001382235.1:c.2302C= NP_001369164.1:p.Arg768=