Canonical Allele Identifier: CA2374774563
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407353A= , CM000682.2:g.63407353A= GRCh38
NC_000020.10:g.62038706A= , CM000682.1:g.62038706A= GRCh37
NC_000020.9:g.61509150A= NCBI36
NG_009004.1:g.70288T=
NG_009004.2:g.70288T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.1964T= ENSP00000516702.1:p.Leu655=
ENST00000359125.7:c.1910T= MANE Select ENSP00000352035.2:p.Leu637=
ENST00000637193.1:c.1307T= ENSP00000490734.1:p.Leu436=
ENST00000637338.1:n.67T=
ENST00000344462.8:c.1817T= ENSP00000339611.4:p.Leu606=
ENST00000357249.6:c.1478T= ENSP00000349789.3:p.Leu493=
ENST00000359125.6:c.1910T= ENSP00000352035.2:p.Leu637=
ENST00000360480.7:c.1826T= ENSP00000353668.3:p.Leu609=
ENST00000370224.5:c.1934T= ENSP00000359244.2:p.Leu645=
ENST00000625514.2:c.1898T= ENSP00000486040.1:p.Leu633=
ENST00000626839.2:c.1856T= ENSP00000486706.1:p.Leu619=
ENST00000629241.2:c.1826T= ENSP00000487142.1:p.Leu609=
ENST00000629676.2:c.1679+6097T= ENSP00000486194.1:n.1679+6097T=
NM_004518.4:c.1826T= NP_004509.2:p.Leu609=
NM_172106.1:c.1856T= NP_742104.1:p.Leu619=
NM_172107.2:c.1910T= NP_742105.1:p.Leu637=
NM_172108.3:c.1817T= NP_742106.1:p.Leu606=
XM_006723787.1:c.1952T= XP_006723850.1:p.Leu651=
XM_011528807.1:c.2018T= XP_011527109.1:p.Leu673=
XM_011528808.1:c.2015T= XP_011527110.1:p.Leu672=
XM_011528809.1:c.1988T= XP_011527111.1:p.Leu663=
XM_011528810.1:c.1964T= XP_011527112.1:p.Leu655=
XM_011528811.1:c.1934T= XP_011527113.1:p.Leu645=
XM_011528812.1:c.1907T= XP_011527114.1:p.Leu636=
XM_011528813.1:c.1892T= XP_011527115.1:p.Leu631=
XM_011528814.1:c.1499T= XP_011527116.1:p.Leu500=
NM_004518.5:c.1826T= NP_004509.2:p.Leu609=
NM_172106.2:c.1856T= NP_742104.1:p.Leu619=
NM_172107.3:c.1910T= NP_742105.1:p.Leu637=
NM_172108.4:c.1817T= NP_742106.1:p.Leu606=
XM_011528810.2:c.1964T= XP_011527112.1:p.Leu655=
XM_011528811.2:c.1934T= XP_011527113.1:p.Leu645=
XM_017027841.2:c.1961T= XP_016883330.1:p.Leu654=
XM_017027842.2:c.1898T= XP_016883331.1:p.Leu633=
XM_017027843.1:c.1895T= XP_016883332.1:p.Leu632=
XM_017027844.2:c.1853T= XP_016883333.1:p.Leu618=
XM_017027845.1:c.926T= XP_016883334.1:p.Leu309=
NM_004518.6:c.1826T= NP_004509.2:p.Leu609=
NM_172106.3:c.1856T= NP_742104.1:p.Leu619=
NM_172107.4:c.1910T= MANE Select NP_742105.1:p.Leu637=
NM_172108.5:c.1817T= NP_742106.1:p.Leu606=
NM_001382235.1:c.1964T= NP_001369164.1:p.Leu655=