Canonical Allele Identifier: CA2374774270
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406848G= , CM000682.2:g.63406848G= GRCh38
NC_000020.10:g.62038201G= , CM000682.1:g.62038201G= GRCh37
NC_000020.9:g.61508645G= NCBI36
NG_009004.1:g.70793C=
NG_009004.2:g.70793C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2469C= ENSP00000516702.1:p.Phe823=
ENST00000359125.7:c.2415C= MANE Select ENSP00000352035.2:p.Phe805=
ENST00000637193.1:c.1812C= ENSP00000490734.1:p.Phe604=
ENST00000344462.8:c.2322C= ENSP00000339611.4:p.Phe774=
ENST00000357249.6:c.1983C= ENSP00000349789.3:p.Phe661=
ENST00000359125.6:c.2415C= ENSP00000352035.2:p.Phe805=
ENST00000360480.7:c.2331C= ENSP00000353668.3:p.Phe777=
ENST00000370224.5:c.2241+198C= ENSP00000359244.2:n.2241+198C=
ENST00000625514.2:c.2205+198C= ENSP00000486040.1:n.2205+198C=
ENST00000626839.2:c.2361C= ENSP00000486706.1:p.Phe787=
ENST00000629241.2:c.2133+198C= ENSP00000487142.1:n.2133+198C=
ENST00000629676.2:c.1680-6005C= ENSP00000486194.1:n.1680-6005C=
NM_004518.4:c.2331C= NP_004509.2:p.Phe777=
NM_172106.1:c.2361C= NP_742104.1:p.Phe787=
NM_172107.2:c.2415C= NP_742105.1:p.Phe805=
NM_172108.3:c.2322C= NP_742106.1:p.Phe774=
XM_006723787.1:c.2457C= XP_006723850.1:p.Phe819=
XM_011528807.1:c.2523C= XP_011527109.1:p.Phe841=
XM_011528808.1:c.2520C= XP_011527110.1:p.Phe840=
XM_011528809.1:c.2493C= XP_011527111.1:p.Phe831=
XM_011528810.1:c.2469C= XP_011527112.1:p.Phe823=
XM_011528811.1:c.2439C= XP_011527113.1:p.Phe813=
XM_011528812.1:c.2412C= XP_011527114.1:p.Phe804=
XM_011528813.1:c.2397C= XP_011527115.1:p.Phe799=
XM_011528814.1:c.2004C= XP_011527116.1:p.Phe668=
NM_004518.5:c.2331C= NP_004509.2:p.Phe777=
NM_172106.2:c.2361C= NP_742104.1:p.Phe787=
NM_172107.3:c.2415C= NP_742105.1:p.Phe805=
NM_172108.4:c.2322C= NP_742106.1:p.Phe774=
XM_011528810.2:c.2469C= XP_011527112.1:p.Phe823=
XM_011528811.2:c.2439C= XP_011527113.1:p.Phe813=
XM_017027841.2:c.2466C= XP_016883330.1:p.Phe822=
XM_017027842.2:c.2403C= XP_016883331.1:p.Phe801=
XM_017027843.1:c.2400C= XP_016883332.1:p.Phe800=
XM_017027844.2:c.2358C= XP_016883333.1:p.Phe786=
XM_017027845.1:c.1431C= XP_016883334.1:p.Phe477=
NM_004518.6:c.2331C= NP_004509.2:p.Phe777=
NM_172106.3:c.2361C= NP_742104.1:p.Phe787=
NM_172107.4:c.2415C= MANE Select NP_742105.1:p.Phe805=
NM_172108.5:c.2322C= NP_742106.1:p.Phe774=
NM_001382235.1:c.2469C= NP_001369164.1:p.Phe823=