Canonical Allele Identifier: CA2374774371
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407020T= , CM000682.2:g.63407020T= GRCh38
NC_000020.10:g.62038373T= , CM000682.1:g.62038373T= GRCh37
NC_000020.9:g.61508817T= NCBI36
NG_009004.1:g.70621A=
NG_009004.2:g.70621A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2297A= ENSP00000516702.1:p.His766=
ENST00000359125.7:c.2243A= MANE Select ENSP00000352035.2:p.His748=
ENST00000637193.1:c.1640A= ENSP00000490734.1:p.His547=
ENST00000344462.8:c.2150A= ENSP00000339611.4:p.His717=
ENST00000357249.6:c.1811A= ENSP00000349789.3:p.His604=
ENST00000359125.6:c.2243A= ENSP00000352035.2:p.His748=
ENST00000360480.7:c.2159A= ENSP00000353668.3:p.His720=
ENST00000370224.5:c.2241+26A= ENSP00000359244.2:n.2241+26A=
ENST00000625514.2:c.2205+26A= ENSP00000486040.1:n.2205+26A=
ENST00000626839.2:c.2189A= ENSP00000486706.1:p.His730=
ENST00000629241.2:c.2133+26A= ENSP00000487142.1:n.2133+26A=
ENST00000629676.2:c.1680-6177A= ENSP00000486194.1:n.1680-6177A=
NM_004518.4:c.2159A= NP_004509.2:p.His720=
NM_172106.1:c.2189A= NP_742104.1:p.His730=
NM_172107.2:c.2243A= NP_742105.1:p.His748=
NM_172108.3:c.2150A= NP_742106.1:p.His717=
XM_006723787.1:c.2285A= XP_006723850.1:p.His762=
XM_011528807.1:c.2351A= XP_011527109.1:p.His784=
XM_011528808.1:c.2348A= XP_011527110.1:p.His783=
XM_011528809.1:c.2321A= XP_011527111.1:p.His774=
XM_011528810.1:c.2297A= XP_011527112.1:p.His766=
XM_011528811.1:c.2267A= XP_011527113.1:p.His756=
XM_011528812.1:c.2240A= XP_011527114.1:p.His747=
XM_011528813.1:c.2225A= XP_011527115.1:p.His742=
XM_011528814.1:c.1832A= XP_011527116.1:p.His611=
NM_004518.5:c.2159A= NP_004509.2:p.His720=
NM_172106.2:c.2189A= NP_742104.1:p.His730=
NM_172107.3:c.2243A= NP_742105.1:p.His748=
NM_172108.4:c.2150A= NP_742106.1:p.His717=
XM_011528810.2:c.2297A= XP_011527112.1:p.His766=
XM_011528811.2:c.2267A= XP_011527113.1:p.His756=
XM_017027841.2:c.2294A= XP_016883330.1:p.His765=
XM_017027842.2:c.2231A= XP_016883331.1:p.His744=
XM_017027843.1:c.2228A= XP_016883332.1:p.His743=
XM_017027844.2:c.2186A= XP_016883333.1:p.His729=
XM_017027845.1:c.1259A= XP_016883334.1:p.His420=
NM_004518.6:c.2159A= NP_004509.2:p.His720=
NM_172106.3:c.2189A= NP_742104.1:p.His730=
NM_172107.4:c.2243A= MANE Select NP_742105.1:p.His748=
NM_172108.5:c.2150A= NP_742106.1:p.His717=
NM_001382235.1:c.2297A= NP_001369164.1:p.His766=