Canonical Allele Identifier: CA2374774491
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407214G= , CM000682.2:g.63407214G= GRCh38
NC_000020.10:g.62038567G= , CM000682.1:g.62038567G= GRCh37
NC_000020.9:g.61509011G= NCBI36
NG_009004.1:g.70427C=
NG_009004.2:g.70427C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2103C= ENSP00000516702.1:p.His701=
ENST00000359125.7:c.2049C= MANE Select ENSP00000352035.2:p.His683=
ENST00000637193.1:c.1446C= ENSP00000490734.1:p.His482=
ENST00000344462.8:c.1956C= ENSP00000339611.4:p.His652=
ENST00000357249.6:c.1617C= ENSP00000349789.3:p.His539=
ENST00000359125.6:c.2049C= ENSP00000352035.2:p.His683=
ENST00000360480.7:c.1965C= ENSP00000353668.3:p.His655=
ENST00000370224.5:c.2073C= ENSP00000359244.2:p.His691=
ENST00000625514.2:c.2037C= ENSP00000486040.1:p.His679=
ENST00000626839.2:c.1995C= ENSP00000486706.1:p.His665=
ENST00000629241.2:c.1965C= ENSP00000487142.1:p.His655=
ENST00000629676.2:c.1679+6236C= ENSP00000486194.1:n.1679+6236C=
NM_004518.4:c.1965C= NP_004509.2:p.His655=
NM_172106.1:c.1995C= NP_742104.1:p.His665=
NM_172107.2:c.2049C= NP_742105.1:p.His683=
NM_172108.3:c.1956C= NP_742106.1:p.His652=
XM_006723787.1:c.2091C= XP_006723850.1:p.His697=
XM_011528807.1:c.2157C= XP_011527109.1:p.His719=
XM_011528808.1:c.2154C= XP_011527110.1:p.His718=
XM_011528809.1:c.2127C= XP_011527111.1:p.His709=
XM_011528810.1:c.2103C= XP_011527112.1:p.His701=
XM_011528811.1:c.2073C= XP_011527113.1:p.His691=
XM_011528812.1:c.2046C= XP_011527114.1:p.His682=
XM_011528813.1:c.2031C= XP_011527115.1:p.His677=
XM_011528814.1:c.1638C= XP_011527116.1:p.His546=
NM_004518.5:c.1965C= NP_004509.2:p.His655=
NM_172106.2:c.1995C= NP_742104.1:p.His665=
NM_172107.3:c.2049C= NP_742105.1:p.His683=
NM_172108.4:c.1956C= NP_742106.1:p.His652=
XM_011528810.2:c.2103C= XP_011527112.1:p.His701=
XM_011528811.2:c.2073C= XP_011527113.1:p.His691=
XM_017027841.2:c.2100C= XP_016883330.1:p.His700=
XM_017027842.2:c.2037C= XP_016883331.1:p.His679=
XM_017027843.1:c.2034C= XP_016883332.1:p.His678=
XM_017027844.2:c.1992C= XP_016883333.1:p.His664=
XM_017027845.1:c.1065C= XP_016883334.1:p.His355=
NM_004518.6:c.1965C= NP_004509.2:p.His655=
NM_172106.3:c.1995C= NP_742104.1:p.His665=
NM_172107.4:c.2049C= MANE Select NP_742105.1:p.His683=
NM_172108.5:c.1956C= NP_742106.1:p.His652=
NM_001382235.1:c.2103C= NP_001369164.1:p.His701=