Canonical Allele Identifier: CA2374774234
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406763T= , CM000682.2:g.63406763T= GRCh38
NC_000020.10:g.62038116T= , CM000682.1:g.62038116T= GRCh37
NC_000020.9:g.61508560T= NCBI36
NG_009004.1:g.70878A=
NG_009004.2:g.70878A=

Transcript Alleles

HGVS Amino-acid change
ENST00000706989.1:c.2554A= ENSP00000516702.1:p.Ile852=
ENST00000359125.7:c.2500A= MANE Select ENSP00000352035.2:p.Ile834=
ENST00000637193.1:c.1897A= ENSP00000490734.1:p.Ile633=
ENST00000344462.8:c.2407A= ENSP00000339611.4:p.Ile803=
ENST00000357249.6:c.2068A= ENSP00000349789.3:p.Ile690=
ENST00000359125.6:c.2500A= ENSP00000352035.2:p.Ile834=
ENST00000360480.7:c.2416A= ENSP00000353668.3:p.Ile806=
ENST00000370224.5:c.2241+283A= ENSP00000359244.2:n.2241+283A=
ENST00000625514.2:c.2205+283A= ENSP00000486040.1:n.2205+283A=
ENST00000626839.2:c.2446A= ENSP00000486706.1:p.Ile816=
ENST00000629241.2:c.2133+283A= ENSP00000487142.1:n.2133+283A=
ENST00000629676.2:c.1680-5920A= ENSP00000486194.1:n.1680-5920A=
NM_004518.4:c.2416A= NP_004509.2:p.Ile806=
NM_172106.1:c.2446A= NP_742104.1:p.Ile816=
NM_172107.2:c.2500A= NP_742105.1:p.Ile834=
NM_172108.3:c.2407A= NP_742106.1:p.Ile803=
XM_006723787.1:c.2542A= XP_006723850.1:p.Ile848=
XM_011528807.1:c.2608A= XP_011527109.1:p.Ile870=
XM_011528808.1:c.2605A= XP_011527110.1:p.Ile869=
XM_011528809.1:c.2578A= XP_011527111.1:p.Ile860=
XM_011528810.1:c.2554A= XP_011527112.1:p.Ile852=
XM_011528811.1:c.2524A= XP_011527113.1:p.Ile842=
XM_011528812.1:c.2497A= XP_011527114.1:p.Ile833=
XM_011528813.1:c.2482A= XP_011527115.1:p.Ile828=
XM_011528814.1:c.2089A= XP_011527116.1:p.Ile697=
NM_004518.5:c.2416A= NP_004509.2:p.Ile806=
NM_172106.2:c.2446A= NP_742104.1:p.Ile816=
NM_172107.3:c.2500A= NP_742105.1:p.Ile834=
NM_172108.4:c.2407A= NP_742106.1:p.Ile803=
XM_011528810.2:c.2554A= XP_011527112.1:p.Ile852=
XM_011528811.2:c.2524A= XP_011527113.1:p.Ile842=
XM_017027841.2:c.2551A= XP_016883330.1:p.Ile851=
XM_017027842.2:c.2488A= XP_016883331.1:p.Ile830=
XM_017027843.1:c.2485A= XP_016883332.1:p.Ile829=
XM_017027844.2:c.2443A= XP_016883333.1:p.Ile815=
XM_017027845.1:c.1516A= XP_016883334.1:p.Ile506=
NM_004518.6:c.2416A= NP_004509.2:p.Ile806=
NM_172106.3:c.2446A= NP_742104.1:p.Ile816=
NM_172107.4:c.2500A= MANE Select NP_742105.1:p.Ile834=
NM_172108.5:c.2407A= NP_742106.1:p.Ile803=
NM_001382235.1:c.2554A= NP_001369164.1:p.Ile852=