Canonical Allele Identifier: CA2374774524
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407284C= , CM000682.2:g.63407284C= GRCh38
NC_000020.10:g.62038637C= , CM000682.1:g.62038637C= GRCh37
NC_000020.9:g.61509081C= NCBI36
NG_009004.1:g.70357G=
NG_009004.2:g.70357G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2033G= ENSP00000516702.1:p.Gly678=
ENST00000359125.7:c.1979G= MANE Select ENSP00000352035.2:p.Gly660=
ENST00000637193.1:c.1376G= ENSP00000490734.1:p.Gly459=
ENST00000344462.8:c.1886G= ENSP00000339611.4:p.Gly629=
ENST00000357249.6:c.1547G= ENSP00000349789.3:p.Gly516=
ENST00000359125.6:c.1979G= ENSP00000352035.2:p.Gly660=
ENST00000360480.7:c.1895G= ENSP00000353668.3:p.Gly632=
ENST00000370224.5:c.2003G= ENSP00000359244.2:p.Gly668=
ENST00000625514.2:c.1967G= ENSP00000486040.1:p.Gly656=
ENST00000626839.2:c.1925G= ENSP00000486706.1:p.Gly642=
ENST00000629241.2:c.1895G= ENSP00000487142.1:p.Gly632=
ENST00000629676.2:c.1679+6166G= ENSP00000486194.1:n.1679+6166G=
NM_004518.4:c.1895G= NP_004509.2:p.Gly632=
NM_172106.1:c.1925G= NP_742104.1:p.Gly642=
NM_172107.2:c.1979G= NP_742105.1:p.Gly660=
NM_172108.3:c.1886G= NP_742106.1:p.Gly629=
XM_006723787.1:c.2021G= XP_006723850.1:p.Gly674=
XM_011528807.1:c.2087G= XP_011527109.1:p.Gly696=
XM_011528808.1:c.2084G= XP_011527110.1:p.Gly695=
XM_011528809.1:c.2057G= XP_011527111.1:p.Gly686=
XM_011528810.1:c.2033G= XP_011527112.1:p.Gly678=
XM_011528811.1:c.2003G= XP_011527113.1:p.Gly668=
XM_011528812.1:c.1976G= XP_011527114.1:p.Gly659=
XM_011528813.1:c.1961G= XP_011527115.1:p.Gly654=
XM_011528814.1:c.1568G= XP_011527116.1:p.Gly523=
NM_004518.5:c.1895G= NP_004509.2:p.Gly632=
NM_172106.2:c.1925G= NP_742104.1:p.Gly642=
NM_172107.3:c.1979G= NP_742105.1:p.Gly660=
NM_172108.4:c.1886G= NP_742106.1:p.Gly629=
XM_011528810.2:c.2033G= XP_011527112.1:p.Gly678=
XM_011528811.2:c.2003G= XP_011527113.1:p.Gly668=
XM_017027841.2:c.2030G= XP_016883330.1:p.Gly677=
XM_017027842.2:c.1967G= XP_016883331.1:p.Gly656=
XM_017027843.1:c.1964G= XP_016883332.1:p.Gly655=
XM_017027844.2:c.1922G= XP_016883333.1:p.Gly641=
XM_017027845.1:c.995G= XP_016883334.1:p.Gly332=
NM_004518.6:c.1895G= NP_004509.2:p.Gly632=
NM_172106.3:c.1925G= NP_742104.1:p.Gly642=
NM_172107.4:c.1979G= MANE Select NP_742105.1:p.Gly660=
NM_172108.5:c.1886G= NP_742106.1:p.Gly629=
NM_001382235.1:c.2033G= NP_001369164.1:p.Gly678=