Canonical Allele Identifier: CA2374774483
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407198T= , CM000682.2:g.63407198T= GRCh38
NC_000020.10:g.62038551T= , CM000682.1:g.62038551T= GRCh37
NC_000020.9:g.61508995T= NCBI36
NG_009004.1:g.70443A=
NG_009004.2:g.70443A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2119A= ENSP00000516702.1:p.Ile707=
ENST00000359125.7:c.2065A= MANE Select ENSP00000352035.2:p.Ile689=
ENST00000637193.1:c.1462A= ENSP00000490734.1:p.Ile488=
ENST00000344462.8:c.1972A= ENSP00000339611.4:p.Ile658=
ENST00000357249.6:c.1633A= ENSP00000349789.3:p.Ile545=
ENST00000359125.6:c.2065A= ENSP00000352035.2:p.Ile689=
ENST00000360480.7:c.1981A= ENSP00000353668.3:p.Ile661=
ENST00000370224.5:c.2089A= ENSP00000359244.2:p.Ile697=
ENST00000625514.2:c.2053A= ENSP00000486040.1:p.Ile685=
ENST00000626839.2:c.2011A= ENSP00000486706.1:p.Ile671=
ENST00000629241.2:c.1981A= ENSP00000487142.1:p.Ile661=
ENST00000629676.2:c.1679+6252A= ENSP00000486194.1:n.1679+6252A=
NM_004518.4:c.1981A= NP_004509.2:p.Ile661=
NM_172106.1:c.2011A= NP_742104.1:p.Ile671=
NM_172107.2:c.2065A= NP_742105.1:p.Ile689=
NM_172108.3:c.1972A= NP_742106.1:p.Ile658=
XM_006723787.1:c.2107A= XP_006723850.1:p.Ile703=
XM_011528807.1:c.2173A= XP_011527109.1:p.Ile725=
XM_011528808.1:c.2170A= XP_011527110.1:p.Ile724=
XM_011528809.1:c.2143A= XP_011527111.1:p.Ile715=
XM_011528810.1:c.2119A= XP_011527112.1:p.Ile707=
XM_011528811.1:c.2089A= XP_011527113.1:p.Ile697=
XM_011528812.1:c.2062A= XP_011527114.1:p.Ile688=
XM_011528813.1:c.2047A= XP_011527115.1:p.Ile683=
XM_011528814.1:c.1654A= XP_011527116.1:p.Ile552=
NM_004518.5:c.1981A= NP_004509.2:p.Ile661=
NM_172106.2:c.2011A= NP_742104.1:p.Ile671=
NM_172107.3:c.2065A= NP_742105.1:p.Ile689=
NM_172108.4:c.1972A= NP_742106.1:p.Ile658=
XM_011528810.2:c.2119A= XP_011527112.1:p.Ile707=
XM_011528811.2:c.2089A= XP_011527113.1:p.Ile697=
XM_017027841.2:c.2116A= XP_016883330.1:p.Ile706=
XM_017027842.2:c.2053A= XP_016883331.1:p.Ile685=
XM_017027843.1:c.2050A= XP_016883332.1:p.Ile684=
XM_017027844.2:c.2008A= XP_016883333.1:p.Ile670=
XM_017027845.1:c.1081A= XP_016883334.1:p.Ile361=
NM_004518.6:c.1981A= NP_004509.2:p.Ile661=
NM_172106.3:c.2011A= NP_742104.1:p.Ile671=
NM_172107.4:c.2065A= MANE Select NP_742105.1:p.Ile689=
NM_172108.5:c.1972A= NP_742106.1:p.Ile658=
NM_001382235.1:c.2119A= NP_001369164.1:p.Ile707=