Canonical Allele Identifier: CA2374774558
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407344A= , CM000682.2:g.63407344A= GRCh38
NC_000020.10:g.62038697A= , CM000682.1:g.62038697A= GRCh37
NC_000020.9:g.61509141A= NCBI36
NG_009004.1:g.70297T=
NG_009004.2:g.70297T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.1973T= ENSP00000516702.1:p.Leu658=
ENST00000359125.7:c.1919T= MANE Select ENSP00000352035.2:p.Leu640=
ENST00000637193.1:c.1316T= ENSP00000490734.1:p.Leu439=
ENST00000637338.1:n.76T=
ENST00000344462.8:c.1826T= ENSP00000339611.4:p.Leu609=
ENST00000357249.6:c.1487T= ENSP00000349789.3:p.Leu496=
ENST00000359125.6:c.1919T= ENSP00000352035.2:p.Leu640=
ENST00000360480.7:c.1835T= ENSP00000353668.3:p.Leu612=
ENST00000370224.5:c.1943T= ENSP00000359244.2:p.Leu648=
ENST00000625514.2:c.1907T= ENSP00000486040.1:p.Leu636=
ENST00000626839.2:c.1865T= ENSP00000486706.1:p.Leu622=
ENST00000629241.2:c.1835T= ENSP00000487142.1:p.Leu612=
ENST00000629676.2:c.1679+6106T= ENSP00000486194.1:n.1679+6106T=
NM_004518.4:c.1835T= NP_004509.2:p.Leu612=
NM_172106.1:c.1865T= NP_742104.1:p.Leu622=
NM_172107.2:c.1919T= NP_742105.1:p.Leu640=
NM_172108.3:c.1826T= NP_742106.1:p.Leu609=
XM_006723787.1:c.1961T= XP_006723850.1:p.Leu654=
XM_011528807.1:c.2027T= XP_011527109.1:p.Leu676=
XM_011528808.1:c.2024T= XP_011527110.1:p.Leu675=
XM_011528809.1:c.1997T= XP_011527111.1:p.Leu666=
XM_011528810.1:c.1973T= XP_011527112.1:p.Leu658=
XM_011528811.1:c.1943T= XP_011527113.1:p.Leu648=
XM_011528812.1:c.1916T= XP_011527114.1:p.Leu639=
XM_011528813.1:c.1901T= XP_011527115.1:p.Leu634=
XM_011528814.1:c.1508T= XP_011527116.1:p.Leu503=
NM_004518.5:c.1835T= NP_004509.2:p.Leu612=
NM_172106.2:c.1865T= NP_742104.1:p.Leu622=
NM_172107.3:c.1919T= NP_742105.1:p.Leu640=
NM_172108.4:c.1826T= NP_742106.1:p.Leu609=
XM_011528810.2:c.1973T= XP_011527112.1:p.Leu658=
XM_011528811.2:c.1943T= XP_011527113.1:p.Leu648=
XM_017027841.2:c.1970T= XP_016883330.1:p.Leu657=
XM_017027842.2:c.1907T= XP_016883331.1:p.Leu636=
XM_017027843.1:c.1904T= XP_016883332.1:p.Leu635=
XM_017027844.2:c.1862T= XP_016883333.1:p.Leu621=
XM_017027845.1:c.935T= XP_016883334.1:p.Leu312=
NM_004518.6:c.1835T= NP_004509.2:p.Leu612=
NM_172106.3:c.1865T= NP_742104.1:p.Leu622=
NM_172107.4:c.1919T= MANE Select NP_742105.1:p.Leu640=
NM_172108.5:c.1826T= NP_742106.1:p.Leu609=
NM_001382235.1:c.1973T= NP_001369164.1:p.Leu658=