Canonical Allele Identifier: CA2374774382
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407035G= , CM000682.2:g.63407035G= GRCh38
NC_000020.10:g.62038388G= , CM000682.1:g.62038388G= GRCh37
NC_000020.9:g.61508832G= NCBI36
NG_009004.1:g.70606C=
NG_009004.2:g.70606C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2282C= ENSP00000516702.1:p.Pro761=
ENST00000359125.7:c.2228C= MANE Select ENSP00000352035.2:p.Pro743=
ENST00000637193.1:c.1625C= ENSP00000490734.1:p.Pro542=
ENST00000344462.8:c.2135C= ENSP00000339611.4:p.Pro712=
ENST00000357249.6:c.1796C= ENSP00000349789.3:p.Pro599=
ENST00000359125.6:c.2228C= ENSP00000352035.2:p.Pro743=
ENST00000360480.7:c.2144C= ENSP00000353668.3:p.Pro715=
ENST00000370224.5:c.2241+11C= ENSP00000359244.2:n.2241+11C=
ENST00000625514.2:c.2205+11C= ENSP00000486040.1:n.2205+11C=
ENST00000626839.2:c.2174C= ENSP00000486706.1:p.Pro725=
ENST00000629241.2:c.2133+11C= ENSP00000487142.1:n.2133+11C=
ENST00000629676.2:c.1680-6192C= ENSP00000486194.1:n.1680-6192C=
NM_004518.4:c.2144C= NP_004509.2:p.Pro715=
NM_172106.1:c.2174C= NP_742104.1:p.Pro725=
NM_172107.2:c.2228C= NP_742105.1:p.Pro743=
NM_172108.3:c.2135C= NP_742106.1:p.Pro712=
XM_006723787.1:c.2270C= XP_006723850.1:p.Pro757=
XM_011528807.1:c.2336C= XP_011527109.1:p.Pro779=
XM_011528808.1:c.2333C= XP_011527110.1:p.Pro778=
XM_011528809.1:c.2306C= XP_011527111.1:p.Pro769=
XM_011528810.1:c.2282C= XP_011527112.1:p.Pro761=
XM_011528811.1:c.2252C= XP_011527113.1:p.Pro751=
XM_011528812.1:c.2225C= XP_011527114.1:p.Pro742=
XM_011528813.1:c.2210C= XP_011527115.1:p.Pro737=
XM_011528814.1:c.1817C= XP_011527116.1:p.Pro606=
NM_004518.5:c.2144C= NP_004509.2:p.Pro715=
NM_172106.2:c.2174C= NP_742104.1:p.Pro725=
NM_172107.3:c.2228C= NP_742105.1:p.Pro743=
NM_172108.4:c.2135C= NP_742106.1:p.Pro712=
XM_011528810.2:c.2282C= XP_011527112.1:p.Pro761=
XM_011528811.2:c.2252C= XP_011527113.1:p.Pro751=
XM_017027841.2:c.2279C= XP_016883330.1:p.Pro760=
XM_017027842.2:c.2216C= XP_016883331.1:p.Pro739=
XM_017027843.1:c.2213C= XP_016883332.1:p.Pro738=
XM_017027844.2:c.2171C= XP_016883333.1:p.Pro724=
XM_017027845.1:c.1244C= XP_016883334.1:p.Pro415=
NM_004518.6:c.2144C= NP_004509.2:p.Pro715=
NM_172106.3:c.2174C= NP_742104.1:p.Pro725=
NM_172107.4:c.2228C= MANE Select NP_742105.1:p.Pro743=
NM_172108.5:c.2135C= NP_742106.1:p.Pro712=
NM_001382235.1:c.2282C= NP_001369164.1:p.Pro761=