Canonical Allele Identifier: CA2374774363
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407004G= , CM000682.2:g.63407004G= GRCh38
NC_000020.10:g.62038357G= , CM000682.1:g.62038357G= GRCh37
NC_000020.9:g.61508801G= NCBI36
NG_009004.1:g.70637C=
NG_009004.2:g.70637C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2313C= ENSP00000516702.1:p.Ser771=
ENST00000359125.7:c.2259C= MANE Select ENSP00000352035.2:p.Ser753=
ENST00000637193.1:c.1656C= ENSP00000490734.1:p.Ser552=
ENST00000344462.8:c.2166C= ENSP00000339611.4:p.Ser722=
ENST00000357249.6:c.1827C= ENSP00000349789.3:p.Ser609=
ENST00000359125.6:c.2259C= ENSP00000352035.2:p.Ser753=
ENST00000360480.7:c.2175C= ENSP00000353668.3:p.Ser725=
ENST00000370224.5:c.2241+42C= ENSP00000359244.2:n.2241+42C=
ENST00000625514.2:c.2205+42C= ENSP00000486040.1:n.2205+42C=
ENST00000626839.2:c.2205C= ENSP00000486706.1:p.Ser735=
ENST00000629241.2:c.2133+42C= ENSP00000487142.1:n.2133+42C=
ENST00000629676.2:c.1680-6161C= ENSP00000486194.1:n.1680-6161C=
NM_004518.4:c.2175C= NP_004509.2:p.Ser725=
NM_172106.1:c.2205C= NP_742104.1:p.Ser735=
NM_172107.2:c.2259C= NP_742105.1:p.Ser753=
NM_172108.3:c.2166C= NP_742106.1:p.Ser722=
XM_006723787.1:c.2301C= XP_006723850.1:p.Ser767=
XM_011528807.1:c.2367C= XP_011527109.1:p.Ser789=
XM_011528808.1:c.2364C= XP_011527110.1:p.Ser788=
XM_011528809.1:c.2337C= XP_011527111.1:p.Ser779=
XM_011528810.1:c.2313C= XP_011527112.1:p.Ser771=
XM_011528811.1:c.2283C= XP_011527113.1:p.Ser761=
XM_011528812.1:c.2256C= XP_011527114.1:p.Ser752=
XM_011528813.1:c.2241C= XP_011527115.1:p.Ser747=
XM_011528814.1:c.1848C= XP_011527116.1:p.Ser616=
NM_004518.5:c.2175C= NP_004509.2:p.Ser725=
NM_172106.2:c.2205C= NP_742104.1:p.Ser735=
NM_172107.3:c.2259C= NP_742105.1:p.Ser753=
NM_172108.4:c.2166C= NP_742106.1:p.Ser722=
XM_011528810.2:c.2313C= XP_011527112.1:p.Ser771=
XM_011528811.2:c.2283C= XP_011527113.1:p.Ser761=
XM_017027841.2:c.2310C= XP_016883330.1:p.Ser770=
XM_017027842.2:c.2247C= XP_016883331.1:p.Ser749=
XM_017027843.1:c.2244C= XP_016883332.1:p.Ser748=
XM_017027844.2:c.2202C= XP_016883333.1:p.Ser734=
XM_017027845.1:c.1275C= XP_016883334.1:p.Ser425=
NM_004518.6:c.2175C= NP_004509.2:p.Ser725=
NM_172106.3:c.2205C= NP_742104.1:p.Ser735=
NM_172107.4:c.2259C= MANE Select NP_742105.1:p.Ser753=
NM_172108.5:c.2166C= NP_742106.1:p.Ser722=
NM_001382235.1:c.2313C= NP_001369164.1:p.Ser771=