Canonical Allele Identifier: CA2374774472
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407182C= , CM000682.2:g.63407182C= GRCh38
NC_000020.10:g.62038535C= , CM000682.1:g.62038535C= GRCh37
NC_000020.9:g.61508979C= NCBI36
NG_009004.1:g.70459G=
NG_009004.2:g.70459G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2135G= ENSP00000516702.1:p.Ser712=
ENST00000359125.7:c.2081G= MANE Select ENSP00000352035.2:p.Ser694=
ENST00000637193.1:c.1478G= ENSP00000490734.1:p.Ser493=
ENST00000344462.8:c.1988G= ENSP00000339611.4:p.Ser663=
ENST00000357249.6:c.1649G= ENSP00000349789.3:p.Ser550=
ENST00000359125.6:c.2081G= ENSP00000352035.2:p.Ser694=
ENST00000360480.7:c.1997G= ENSP00000353668.3:p.Ser666=
ENST00000370224.5:c.2105G= ENSP00000359244.2:p.Ser702=
ENST00000625514.2:c.2069G= ENSP00000486040.1:p.Ser690=
ENST00000626839.2:c.2027G= ENSP00000486706.1:p.Ser676=
ENST00000629241.2:c.1997G= ENSP00000487142.1:p.Ser666=
ENST00000629676.2:c.1679+6268G= ENSP00000486194.1:n.1679+6268G=
NM_004518.4:c.1997G= NP_004509.2:p.Ser666=
NM_172106.1:c.2027G= NP_742104.1:p.Ser676=
NM_172107.2:c.2081G= NP_742105.1:p.Ser694=
NM_172108.3:c.1988G= NP_742106.1:p.Ser663=
XM_006723787.1:c.2123G= XP_006723850.1:p.Ser708=
XM_011528807.1:c.2189G= XP_011527109.1:p.Ser730=
XM_011528808.1:c.2186G= XP_011527110.1:p.Ser729=
XM_011528809.1:c.2159G= XP_011527111.1:p.Ser720=
XM_011528810.1:c.2135G= XP_011527112.1:p.Ser712=
XM_011528811.1:c.2105G= XP_011527113.1:p.Ser702=
XM_011528812.1:c.2078G= XP_011527114.1:p.Ser693=
XM_011528813.1:c.2063G= XP_011527115.1:p.Ser688=
XM_011528814.1:c.1670G= XP_011527116.1:p.Ser557=
NM_004518.5:c.1997G= NP_004509.2:p.Ser666=
NM_172106.2:c.2027G= NP_742104.1:p.Ser676=
NM_172107.3:c.2081G= NP_742105.1:p.Ser694=
NM_172108.4:c.1988G= NP_742106.1:p.Ser663=
XM_011528810.2:c.2135G= XP_011527112.1:p.Ser712=
XM_011528811.2:c.2105G= XP_011527113.1:p.Ser702=
XM_017027841.2:c.2132G= XP_016883330.1:p.Ser711=
XM_017027842.2:c.2069G= XP_016883331.1:p.Ser690=
XM_017027843.1:c.2066G= XP_016883332.1:p.Ser689=
XM_017027844.2:c.2024G= XP_016883333.1:p.Ser675=
XM_017027845.1:c.1097G= XP_016883334.1:p.Ser366=
NM_004518.6:c.1997G= NP_004509.2:p.Ser666=
NM_172106.3:c.2027G= NP_742104.1:p.Ser676=
NM_172107.4:c.2081G= MANE Select NP_742105.1:p.Ser694=
NM_172108.5:c.1988G= NP_742106.1:p.Ser663=
NM_001382235.1:c.2135G= NP_001369164.1:p.Ser712=