Canonical Allele Identifier: CA2374774511
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63407256C= , CM000682.2:g.63407256C= GRCh38
NC_000020.10:g.62038609C= , CM000682.1:g.62038609C= GRCh37
NC_000020.9:g.61509053C= NCBI36
NG_009004.1:g.70385G=
NG_009004.2:g.70385G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2061G= ENSP00000516702.1:p.Pro687=
ENST00000359125.7:c.2007G= MANE Select ENSP00000352035.2:p.Pro669=
ENST00000637193.1:c.1404G= ENSP00000490734.1:p.Pro468=
ENST00000344462.8:c.1914G= ENSP00000339611.4:p.Pro638=
ENST00000357249.6:c.1575G= ENSP00000349789.3:p.Pro525=
ENST00000359125.6:c.2007G= ENSP00000352035.2:p.Pro669=
ENST00000360480.7:c.1923G= ENSP00000353668.3:p.Pro641=
ENST00000370224.5:c.2031G= ENSP00000359244.2:p.Pro677=
ENST00000625514.2:c.1995G= ENSP00000486040.1:p.Pro665=
ENST00000626839.2:c.1953G= ENSP00000486706.1:p.Pro651=
ENST00000629241.2:c.1923G= ENSP00000487142.1:p.Pro641=
ENST00000629676.2:c.1679+6194G= ENSP00000486194.1:n.1679+6194G=
NM_004518.4:c.1923G= NP_004509.2:p.Pro641=
NM_172106.1:c.1953G= NP_742104.1:p.Pro651=
NM_172107.2:c.2007G= NP_742105.1:p.Pro669=
NM_172108.3:c.1914G= NP_742106.1:p.Pro638=
XM_006723787.1:c.2049G= XP_006723850.1:p.Pro683=
XM_011528807.1:c.2115G= XP_011527109.1:p.Pro705=
XM_011528808.1:c.2112G= XP_011527110.1:p.Pro704=
XM_011528809.1:c.2085G= XP_011527111.1:p.Pro695=
XM_011528810.1:c.2061G= XP_011527112.1:p.Pro687=
XM_011528811.1:c.2031G= XP_011527113.1:p.Pro677=
XM_011528812.1:c.2004G= XP_011527114.1:p.Pro668=
XM_011528813.1:c.1989G= XP_011527115.1:p.Pro663=
XM_011528814.1:c.1596G= XP_011527116.1:p.Pro532=
NM_004518.5:c.1923G= NP_004509.2:p.Pro641=
NM_172106.2:c.1953G= NP_742104.1:p.Pro651=
NM_172107.3:c.2007G= NP_742105.1:p.Pro669=
NM_172108.4:c.1914G= NP_742106.1:p.Pro638=
XM_011528810.2:c.2061G= XP_011527112.1:p.Pro687=
XM_011528811.2:c.2031G= XP_011527113.1:p.Pro677=
XM_017027841.2:c.2058G= XP_016883330.1:p.Pro686=
XM_017027842.2:c.1995G= XP_016883331.1:p.Pro665=
XM_017027843.1:c.1992G= XP_016883332.1:p.Pro664=
XM_017027844.2:c.1950G= XP_016883333.1:p.Pro650=
XM_017027845.1:c.1023G= XP_016883334.1:p.Pro341=
NM_004518.6:c.1923G= NP_004509.2:p.Pro641=
NM_172106.3:c.1953G= NP_742104.1:p.Pro651=
NM_172107.4:c.2007G= MANE Select NP_742105.1:p.Pro669=
NM_172108.5:c.1914G= NP_742106.1:p.Pro638=
NM_001382235.1:c.2061G= NP_001369164.1:p.Pro687=