Canonical Allele Identifier: CA2374774376
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407029G= , CM000682.2:g.63407029G= GRCh38
NC_000020.10:g.62038382G= , CM000682.1:g.62038382G= GRCh37
NC_000020.9:g.61508826G= NCBI36
NG_009004.1:g.70612C=
NG_009004.2:g.70612C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2288C= ENSP00000516702.1:p.Pro763=
ENST00000359125.7:c.2234C= MANE Select ENSP00000352035.2:p.Pro745=
ENST00000637193.1:c.1631C= ENSP00000490734.1:p.Pro544=
ENST00000344462.8:c.2141C= ENSP00000339611.4:p.Pro714=
ENST00000357249.6:c.1802C= ENSP00000349789.3:p.Pro601=
ENST00000359125.6:c.2234C= ENSP00000352035.2:p.Pro745=
ENST00000360480.7:c.2150C= ENSP00000353668.3:p.Pro717=
ENST00000370224.5:c.2241+17C= ENSP00000359244.2:n.2241+17C=
ENST00000625514.2:c.2205+17C= ENSP00000486040.1:n.2205+17C=
ENST00000626839.2:c.2180C= ENSP00000486706.1:p.Pro727=
ENST00000629241.2:c.2133+17C= ENSP00000487142.1:n.2133+17C=
ENST00000629676.2:c.1680-6186C= ENSP00000486194.1:n.1680-6186C=
NM_004518.4:c.2150C= NP_004509.2:p.Pro717=
NM_172106.1:c.2180C= NP_742104.1:p.Pro727=
NM_172107.2:c.2234C= NP_742105.1:p.Pro745=
NM_172108.3:c.2141C= NP_742106.1:p.Pro714=
XM_006723787.1:c.2276C= XP_006723850.1:p.Pro759=
XM_011528807.1:c.2342C= XP_011527109.1:p.Pro781=
XM_011528808.1:c.2339C= XP_011527110.1:p.Pro780=
XM_011528809.1:c.2312C= XP_011527111.1:p.Pro771=
XM_011528810.1:c.2288C= XP_011527112.1:p.Pro763=
XM_011528811.1:c.2258C= XP_011527113.1:p.Pro753=
XM_011528812.1:c.2231C= XP_011527114.1:p.Pro744=
XM_011528813.1:c.2216C= XP_011527115.1:p.Pro739=
XM_011528814.1:c.1823C= XP_011527116.1:p.Pro608=
NM_004518.5:c.2150C= NP_004509.2:p.Pro717=
NM_172106.2:c.2180C= NP_742104.1:p.Pro727=
NM_172107.3:c.2234C= NP_742105.1:p.Pro745=
NM_172108.4:c.2141C= NP_742106.1:p.Pro714=
XM_011528810.2:c.2288C= XP_011527112.1:p.Pro763=
XM_011528811.2:c.2258C= XP_011527113.1:p.Pro753=
XM_017027841.2:c.2285C= XP_016883330.1:p.Pro762=
XM_017027842.2:c.2222C= XP_016883331.1:p.Pro741=
XM_017027843.1:c.2219C= XP_016883332.1:p.Pro740=
XM_017027844.2:c.2177C= XP_016883333.1:p.Pro726=
XM_017027845.1:c.1250C= XP_016883334.1:p.Pro417=
NM_004518.6:c.2150C= NP_004509.2:p.Pro717=
NM_172106.3:c.2180C= NP_742104.1:p.Pro727=
NM_172107.4:c.2234C= MANE Select NP_742105.1:p.Pro745=
NM_172108.5:c.2141C= NP_742106.1:p.Pro714=
NM_001382235.1:c.2288C= NP_001369164.1:p.Pro763=