Canonical Allele Identifier: CA409637234
Gene: KCNQ2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406857G>T , CM000682.2:g.63406857G>T GRCh38
NC_000020.10:g.62038210G>T , CM000682.1:g.62038210G>T GRCh37
NC_000020.9:g.61508654G>T NCBI36
NG_009004.1:g.70784C>A
NG_009004.2:g.70784C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2460C>A ENSP00000516702.1:p.Phe820Leu
ENST00000359125.7:c.2406C>A MANE Select ENSP00000352035.2:p.Phe802Leu
ENST00000637193.1:c.1803C>A ENSP00000490734.1:p.Phe601Leu
ENST00000344462.8:c.2313C>A ENSP00000339611.4:p.Phe771Leu
ENST00000357249.6:c.1974C>A ENSP00000349789.3:p.Phe658Leu
ENST00000359125.6:c.2406C>A ENSP00000352035.2:p.Phe802Leu
ENST00000360480.7:c.2322C>A ENSP00000353668.3:p.Phe774Leu
ENST00000370224.5:c.2241+189C>A ENSP00000359244.2:n.2241+189C>A
ENST00000625514.2:c.2205+189C>A ENSP00000486040.1:n.2205+189C>A
ENST00000626839.2:c.2352C>A ENSP00000486706.1:p.Phe784Leu
ENST00000629241.2:c.2133+189C>A ENSP00000487142.1:n.2133+189C>A
ENST00000629676.2:c.1680-6014C>A ENSP00000486194.1:n.1680-6014C>A
NM_004518.4:c.2322C>A NP_004509.2:p.Phe774Leu
NM_172106.1:c.2352C>A NP_742104.1:p.Phe784Leu
NM_172107.2:c.2406C>A NP_742105.1:p.Phe802Leu
NM_172108.3:c.2313C>A NP_742106.1:p.Phe771Leu
XM_006723787.1:c.2448C>A XP_006723850.1:p.Phe816Leu
XM_011528807.1:c.2514C>A XP_011527109.1:p.Phe838Leu
XM_011528808.1:c.2511C>A XP_011527110.1:p.Phe837Leu
XM_011528809.1:c.2484C>A XP_011527111.1:p.Phe828Leu
XM_011528810.1:c.2460C>A XP_011527112.1:p.Phe820Leu
XM_011528811.1:c.2430C>A XP_011527113.1:p.Phe810Leu
XM_011528812.1:c.2403C>A XP_011527114.1:p.Phe801Leu
XM_011528813.1:c.2388C>A XP_011527115.1:p.Phe796Leu
XM_011528814.1:c.1995C>A XP_011527116.1:p.Phe665Leu
NM_004518.5:c.2322C>A NP_004509.2:p.Phe774Leu
NM_172106.2:c.2352C>A NP_742104.1:p.Phe784Leu
NM_172107.3:c.2406C>A NP_742105.1:p.Phe802Leu
NM_172108.4:c.2313C>A NP_742106.1:p.Phe771Leu
XM_011528810.2:c.2460C>A XP_011527112.1:p.Phe820Leu
XM_011528811.2:c.2430C>A XP_011527113.1:p.Phe810Leu
XM_017027841.2:c.2457C>A XP_016883330.1:p.Phe819Leu
XM_017027842.2:c.2394C>A XP_016883331.1:p.Phe798Leu
XM_017027843.1:c.2391C>A XP_016883332.1:p.Phe797Leu
XM_017027844.2:c.2349C>A XP_016883333.1:p.Phe783Leu
XM_017027845.1:c.1422C>A XP_016883334.1:p.Phe474Leu
NM_004518.6:c.2322C>A NP_004509.2:p.Phe774Leu
NM_172106.3:c.2352C>A NP_742104.1:p.Phe784Leu
NM_172107.4:c.2406C>A MANE Select NP_742105.1:p.Phe802Leu
NM_172108.5:c.2313C>A NP_742106.1:p.Phe771Leu
NM_001382235.1:c.2460C>A NP_001369164.1:p.Phe820Leu