Canonical Allele Identifier: CA2374774315
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406933G= , CM000682.2:g.63406933G= GRCh38
NC_000020.10:g.62038286G= , CM000682.1:g.62038286G= GRCh37
NC_000020.9:g.61508730G= NCBI36
NG_009004.1:g.70708C=
NG_009004.2:g.70708C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2384C= ENSP00000516702.1:p.Pro795=
ENST00000359125.7:c.2330C= MANE Select ENSP00000352035.2:p.Pro777=
ENST00000637193.1:c.1727C= ENSP00000490734.1:p.Pro576=
ENST00000344462.8:c.2237C= ENSP00000339611.4:p.Pro746=
ENST00000357249.6:c.1898C= ENSP00000349789.3:p.Pro633=
ENST00000359125.6:c.2330C= ENSP00000352035.2:p.Pro777=
ENST00000360480.7:c.2246C= ENSP00000353668.3:p.Pro749=
ENST00000370224.5:c.2241+113C= ENSP00000359244.2:n.2241+113C=
ENST00000625514.2:c.2205+113C= ENSP00000486040.1:n.2205+113C=
ENST00000626839.2:c.2276C= ENSP00000486706.1:p.Pro759=
ENST00000629241.2:c.2133+113C= ENSP00000487142.1:n.2133+113C=
ENST00000629676.2:c.1680-6090C= ENSP00000486194.1:n.1680-6090C=
NM_004518.4:c.2246C= NP_004509.2:p.Pro749=
NM_172106.1:c.2276C= NP_742104.1:p.Pro759=
NM_172107.2:c.2330C= NP_742105.1:p.Pro777=
NM_172108.3:c.2237C= NP_742106.1:p.Pro746=
XM_006723787.1:c.2372C= XP_006723850.1:p.Pro791=
XM_011528807.1:c.2438C= XP_011527109.1:p.Pro813=
XM_011528808.1:c.2435C= XP_011527110.1:p.Pro812=
XM_011528809.1:c.2408C= XP_011527111.1:p.Pro803=
XM_011528810.1:c.2384C= XP_011527112.1:p.Pro795=
XM_011528811.1:c.2354C= XP_011527113.1:p.Pro785=
XM_011528812.1:c.2327C= XP_011527114.1:p.Pro776=
XM_011528813.1:c.2312C= XP_011527115.1:p.Pro771=
XM_011528814.1:c.1919C= XP_011527116.1:p.Pro640=
NM_004518.5:c.2246C= NP_004509.2:p.Pro749=
NM_172106.2:c.2276C= NP_742104.1:p.Pro759=
NM_172107.3:c.2330C= NP_742105.1:p.Pro777=
NM_172108.4:c.2237C= NP_742106.1:p.Pro746=
XM_011528810.2:c.2384C= XP_011527112.1:p.Pro795=
XM_011528811.2:c.2354C= XP_011527113.1:p.Pro785=
XM_017027841.2:c.2381C= XP_016883330.1:p.Pro794=
XM_017027842.2:c.2318C= XP_016883331.1:p.Pro773=
XM_017027843.1:c.2315C= XP_016883332.1:p.Pro772=
XM_017027844.2:c.2273C= XP_016883333.1:p.Pro758=
XM_017027845.1:c.1346C= XP_016883334.1:p.Pro449=
NM_004518.6:c.2246C= NP_004509.2:p.Pro749=
NM_172106.3:c.2276C= NP_742104.1:p.Pro759=
NM_172107.4:c.2330C= MANE Select NP_742105.1:p.Pro777=
NM_172108.5:c.2237C= NP_742106.1:p.Pro746=
NM_001382235.1:c.2384C= NP_001369164.1:p.Pro795=