Canonical Allele Identifier: CA2374774283
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63406877C= , CM000682.2:g.63406877C= GRCh38
NC_000020.10:g.62038230C= , CM000682.1:g.62038230C= GRCh37
NC_000020.9:g.61508674C= NCBI36
NG_009004.1:g.70764G=
NG_009004.2:g.70764G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.2440G= ENSP00000516702.1:p.Glu814=
ENST00000359125.7:c.2386G= MANE Select ENSP00000352035.2:p.Glu796=
ENST00000637193.1:c.1783G= ENSP00000490734.1:p.Glu595=
ENST00000344462.8:c.2293G= ENSP00000339611.4:p.Glu765=
ENST00000357249.6:c.1954G= ENSP00000349789.3:p.Glu652=
ENST00000359125.6:c.2386G= ENSP00000352035.2:p.Glu796=
ENST00000360480.7:c.2302G= ENSP00000353668.3:p.Glu768=
ENST00000370224.5:c.2241+169G= ENSP00000359244.2:n.2241+169G=
ENST00000625514.2:c.2205+169G= ENSP00000486040.1:n.2205+169G=
ENST00000626839.2:c.2332G= ENSP00000486706.1:p.Glu778=
ENST00000629241.2:c.2133+169G= ENSP00000487142.1:n.2133+169G=
ENST00000629676.2:c.1680-6034G= ENSP00000486194.1:n.1680-6034G=
NM_004518.4:c.2302G= NP_004509.2:p.Glu768=
NM_172106.1:c.2332G= NP_742104.1:p.Glu778=
NM_172107.2:c.2386G= NP_742105.1:p.Glu796=
NM_172108.3:c.2293G= NP_742106.1:p.Glu765=
XM_006723787.1:c.2428G= XP_006723850.1:p.Glu810=
XM_011528807.1:c.2494G= XP_011527109.1:p.Glu832=
XM_011528808.1:c.2491G= XP_011527110.1:p.Glu831=
XM_011528809.1:c.2464G= XP_011527111.1:p.Glu822=
XM_011528810.1:c.2440G= XP_011527112.1:p.Glu814=
XM_011528811.1:c.2410G= XP_011527113.1:p.Glu804=
XM_011528812.1:c.2383G= XP_011527114.1:p.Glu795=
XM_011528813.1:c.2368G= XP_011527115.1:p.Glu790=
XM_011528814.1:c.1975G= XP_011527116.1:p.Glu659=
NM_004518.5:c.2302G= NP_004509.2:p.Glu768=
NM_172106.2:c.2332G= NP_742104.1:p.Glu778=
NM_172107.3:c.2386G= NP_742105.1:p.Glu796=
NM_172108.4:c.2293G= NP_742106.1:p.Glu765=
XM_011528810.2:c.2440G= XP_011527112.1:p.Glu814=
XM_011528811.2:c.2410G= XP_011527113.1:p.Glu804=
XM_017027841.2:c.2437G= XP_016883330.1:p.Glu813=
XM_017027842.2:c.2374G= XP_016883331.1:p.Glu792=
XM_017027843.1:c.2371G= XP_016883332.1:p.Glu791=
XM_017027844.2:c.2329G= XP_016883333.1:p.Glu777=
XM_017027845.1:c.1402G= XP_016883334.1:p.Glu468=
NM_004518.6:c.2302G= NP_004509.2:p.Glu768=
NM_172106.3:c.2332G= NP_742104.1:p.Glu778=
NM_172107.4:c.2386G= MANE Select NP_742105.1:p.Glu796=
NM_172108.5:c.2293G= NP_742106.1:p.Glu765=
NM_001382235.1:c.2440G= NP_001369164.1:p.Glu814=