Canonical Allele Identifier: CA2374774249
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406793C= , CM000682.2:g.63406793C= GRCh38
NC_000020.10:g.62038146C= , CM000682.1:g.62038146C= GRCh37
NC_000020.9:g.61508590C= NCBI36
NG_009004.1:g.70848G=
NG_009004.2:g.70848G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2524G= ENSP00000516702.1:p.Val842=
ENST00000359125.7:c.2470G= MANE Select ENSP00000352035.2:p.Val824=
ENST00000637193.1:c.1867G= ENSP00000490734.1:p.Val623=
ENST00000344462.8:c.2377G= ENSP00000339611.4:p.Val793=
ENST00000357249.6:c.2038G= ENSP00000349789.3:p.Val680=
ENST00000359125.6:c.2470G= ENSP00000352035.2:p.Val824=
ENST00000360480.7:c.2386G= ENSP00000353668.3:p.Val796=
ENST00000370224.5:c.2241+253G= ENSP00000359244.2:n.2241+253G=
ENST00000625514.2:c.2205+253G= ENSP00000486040.1:n.2205+253G=
ENST00000626839.2:c.2416G= ENSP00000486706.1:p.Val806=
ENST00000629241.2:c.2133+253G= ENSP00000487142.1:n.2133+253G=
ENST00000629676.2:c.1680-5950G= ENSP00000486194.1:n.1680-5950G=
NM_004518.4:c.2386G= NP_004509.2:p.Val796=
NM_172106.1:c.2416G= NP_742104.1:p.Val806=
NM_172107.2:c.2470G= NP_742105.1:p.Val824=
NM_172108.3:c.2377G= NP_742106.1:p.Val793=
XM_006723787.1:c.2512G= XP_006723850.1:p.Val838=
XM_011528807.1:c.2578G= XP_011527109.1:p.Val860=
XM_011528808.1:c.2575G= XP_011527110.1:p.Val859=
XM_011528809.1:c.2548G= XP_011527111.1:p.Val850=
XM_011528810.1:c.2524G= XP_011527112.1:p.Val842=
XM_011528811.1:c.2494G= XP_011527113.1:p.Val832=
XM_011528812.1:c.2467G= XP_011527114.1:p.Val823=
XM_011528813.1:c.2452G= XP_011527115.1:p.Val818=
XM_011528814.1:c.2059G= XP_011527116.1:p.Val687=
NM_004518.5:c.2386G= NP_004509.2:p.Val796=
NM_172106.2:c.2416G= NP_742104.1:p.Val806=
NM_172107.3:c.2470G= NP_742105.1:p.Val824=
NM_172108.4:c.2377G= NP_742106.1:p.Val793=
XM_011528810.2:c.2524G= XP_011527112.1:p.Val842=
XM_011528811.2:c.2494G= XP_011527113.1:p.Val832=
XM_017027841.2:c.2521G= XP_016883330.1:p.Val841=
XM_017027842.2:c.2458G= XP_016883331.1:p.Val820=
XM_017027843.1:c.2455G= XP_016883332.1:p.Val819=
XM_017027844.2:c.2413G= XP_016883333.1:p.Val805=
XM_017027845.1:c.1486G= XP_016883334.1:p.Val496=
NM_004518.6:c.2386G= NP_004509.2:p.Val796=
NM_172106.3:c.2416G= NP_742104.1:p.Val806=
NM_172107.4:c.2470G= MANE Select NP_742105.1:p.Val824=
NM_172108.5:c.2377G= NP_742106.1:p.Val793=
NM_001382235.1:c.2524G= NP_001369164.1:p.Val842=