Canonical Allele Identifier: CA2374774351
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406986G= , CM000682.2:g.63406986G= GRCh38
NC_000020.10:g.62038339G= , CM000682.1:g.62038339G= GRCh37
NC_000020.9:g.61508783G= NCBI36
NG_009004.1:g.70655C=
NG_009004.2:g.70655C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2331C= ENSP00000516702.1:p.Asn777=
ENST00000359125.7:c.2277C= MANE Select ENSP00000352035.2:p.Asn759=
ENST00000637193.1:c.1674C= ENSP00000490734.1:p.Asn558=
ENST00000344462.8:c.2184C= ENSP00000339611.4:p.Asn728=
ENST00000357249.6:c.1845C= ENSP00000349789.3:p.Asn615=
ENST00000359125.6:c.2277C= ENSP00000352035.2:p.Asn759=
ENST00000360480.7:c.2193C= ENSP00000353668.3:p.Asn731=
ENST00000370224.5:c.2241+60C= ENSP00000359244.2:n.2241+60C=
ENST00000625514.2:c.2205+60C= ENSP00000486040.1:n.2205+60C=
ENST00000626839.2:c.2223C= ENSP00000486706.1:p.Asn741=
ENST00000629241.2:c.2133+60C= ENSP00000487142.1:n.2133+60C=
ENST00000629676.2:c.1680-6143C= ENSP00000486194.1:n.1680-6143C=
NM_004518.4:c.2193C= NP_004509.2:p.Asn731=
NM_172106.1:c.2223C= NP_742104.1:p.Asn741=
NM_172107.2:c.2277C= NP_742105.1:p.Asn759=
NM_172108.3:c.2184C= NP_742106.1:p.Asn728=
XM_006723787.1:c.2319C= XP_006723850.1:p.Asn773=
XM_011528807.1:c.2385C= XP_011527109.1:p.Asn795=
XM_011528808.1:c.2382C= XP_011527110.1:p.Asn794=
XM_011528809.1:c.2355C= XP_011527111.1:p.Asn785=
XM_011528810.1:c.2331C= XP_011527112.1:p.Asn777=
XM_011528811.1:c.2301C= XP_011527113.1:p.Asn767=
XM_011528812.1:c.2274C= XP_011527114.1:p.Asn758=
XM_011528813.1:c.2259C= XP_011527115.1:p.Asn753=
XM_011528814.1:c.1866C= XP_011527116.1:p.Asn622=
NM_004518.5:c.2193C= NP_004509.2:p.Asn731=
NM_172106.2:c.2223C= NP_742104.1:p.Asn741=
NM_172107.3:c.2277C= NP_742105.1:p.Asn759=
NM_172108.4:c.2184C= NP_742106.1:p.Asn728=
XM_011528810.2:c.2331C= XP_011527112.1:p.Asn777=
XM_011528811.2:c.2301C= XP_011527113.1:p.Asn767=
XM_017027841.2:c.2328C= XP_016883330.1:p.Asn776=
XM_017027842.2:c.2265C= XP_016883331.1:p.Asn755=
XM_017027843.1:c.2262C= XP_016883332.1:p.Asn754=
XM_017027844.2:c.2220C= XP_016883333.1:p.Asn740=
XM_017027845.1:c.1293C= XP_016883334.1:p.Asn431=
NM_004518.6:c.2193C= NP_004509.2:p.Asn731=
NM_172106.3:c.2223C= NP_742104.1:p.Asn741=
NM_172107.4:c.2277C= MANE Select NP_742105.1:p.Asn759=
NM_172108.5:c.2184C= NP_742106.1:p.Asn728=
NM_001382235.1:c.2331C= NP_001369164.1:p.Asn777=