Canonical Allele Identifier: CA2374796000
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63444367_63444372delinsTCGCGG , CM000682.2:g.63444367_63444372delinsTCGCGG GRCh38
NC_000020.10:g.62075720_62075725delinsTCGCGG , CM000682.1:g.62075720_62075725delinsTCGCGG GRCh37
NC_000020.9:g.61546164_61546169delinsTCGCGG NCBI36
NG_009004.1:g.33269_33274delinsCCGCGA
NG_009004.2:g.33269_33274delinsCCGCGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.690+287_690+292delinsCCGCGA ENSP00000516702.1:n.690+287_690+292delinsCCGCGA
ENST00000344425.8:c.690+287_690+292delinsCCGCGA ENSP00000345523.5:n.690+287_690+292delinsCCGCGA
ENST00000359125.7:c.690+287_690+292delinsCCGCGA MANE Select ENSP00000352035.2:n.690+287_690+292delinsCCGCGA
ENST00000636255.1:n.428+287_428+292delinsCCGCGA
ENST00000636873.1:n.84+287_84+292delinsCCGCGA
ENST00000637193.1:c.171+287_171+292delinsCCGCGA ENSP00000490734.1:n.171+287_171+292delinsCCGCGA
ENST00000344425.7:c.690+287_690+292delinsCCGCGA ENSP00000345523.5:n.690+287_690+292delinsCCGCGA
ENST00000344462.8:c.690+287_690+292delinsCCGCGA ENSP00000339611.4:n.690+287_690+292delinsCCGCGA
ENST00000357249.6:c.348+287_348+292delinsCCGCGA ENSP00000349789.3:n.348+287_348+292delinsCCGCGA
ENST00000359125.6:c.690+287_690+292delinsCCGCGA ENSP00000352035.2:n.690+287_690+292delinsCCGCGA
ENST00000360480.7:c.690+287_690+292delinsCCGCGA ENSP00000353668.3:n.690+287_690+292delinsCCGCGA
ENST00000370221.3:n.816+287_816+292delinsCCGCGA
ENST00000370224.5:c.690+287_690+292delinsCCGCGA ENSP00000359244.2:n.690+287_690+292delinsCCGCGA
ENST00000625514.2:c.690+287_690+292delinsCCGCGA ENSP00000486040.1:n.690+287_690+292delinsCCGCGA
ENST00000626313.1:n.532+287_532+292delinsCCGCGA
ENST00000626684.1:c.55+287_55+292delinsCCGCGA
ENST00000626839.2:c.690+287_690+292delinsCCGCGA ENSP00000486706.1:n.690+287_690+292delinsCCGCGA
ENST00000629241.2:c.690+287_690+292delinsCCGCGA ENSP00000487142.1:n.690+287_690+292delinsCCGCGA
ENST00000629498.2:c.111+287_111+292delinsCCGCGA ENSP00000486509.1:n.111+287_111+292delinsCCGCGA
ENST00000629676.2:c.690+287_690+292delinsCCGCGA ENSP00000486194.1:n.690+287_690+292delinsCCGCGA
ENST00000630274.2:n.515+287_515+292delinsCCGCGA
NM_004518.4:c.690+287_690+292delinsCCGCGA NP_004509.2:n.690+287_690+292delinsCCGCGA
NM_172106.1:c.690+287_690+292delinsCCGCGA NP_742104.1:n.690+287_690+292delinsCCGCGA
NM_172107.2:c.690+287_690+292delinsCCGCGA NP_742105.1:n.690+287_690+292delinsCCGCGA
NM_172108.3:c.690+287_690+292delinsCCGCGA NP_742106.1:n.690+287_690+292delinsCCGCGA
NM_172109.1:c.690+287_690+292delinsCCGCGA NP_742107.1:n.690+287_690+292delinsCCGCGA
XM_006723787.1:c.690+287_690+292delinsCCGCGA XP_006723850.1:n.690+287_690+292delinsCCGCGA
XM_011528807.1:c.690+287_690+292delinsCCGCGA XP_011527109.1:n.690+287_690+292delinsCCGCGA
XM_011528808.1:c.690+287_690+292delinsCCGCGA XP_011527110.1:n.690+287_690+292delinsCCGCGA
XM_011528809.1:c.690+287_690+292delinsCCGCGA XP_011527111.1:n.690+287_690+292delinsCCGCGA
XM_011528810.1:c.690+287_690+292delinsCCGCGA XP_011527112.1:n.690+287_690+292delinsCCGCGA
XM_011528811.1:c.690+287_690+292delinsCCGCGA XP_011527113.1:n.690+287_690+292delinsCCGCGA
XM_011528812.1:c.690+287_690+292delinsCCGCGA XP_011527114.1:n.690+287_690+292delinsCCGCGA
XM_011528813.1:c.690+287_690+292delinsCCGCGA XP_011527115.1:n.690+287_690+292delinsCCGCGA
XM_011528814.1:c.171+287_171+292delinsCCGCGA XP_011527116.1:n.171+287_171+292delinsCCGCGA
XM_011528815.1:c.690+287_690+292delinsCCGCGA XP_011527117.1:n.690+287_690+292delinsCCGCGA
XM_011528816.1:c.690+287_690+292delinsCCGCGA XP_011527118.1:n.690+287_690+292delinsCCGCGA
NM_004518.5:c.690+287_690+292delinsCCGCGA NP_004509.2:n.690+287_690+292delinsCCGCGA
NM_172106.2:c.690+287_690+292delinsCCGCGA NP_742104.1:n.690+287_690+292delinsCCGCGA
NM_172107.3:c.690+287_690+292delinsCCGCGA NP_742105.1:n.690+287_690+292delinsCCGCGA
NM_172108.4:c.690+287_690+292delinsCCGCGA NP_742106.1:n.690+287_690+292delinsCCGCGA
NM_172109.2:c.690+287_690+292delinsCCGCGA NP_742107.1:n.690+287_690+292delinsCCGCGA
XM_011528810.2:c.690+287_690+292delinsCCGCGA XP_011527112.1:n.690+287_690+292delinsCCGCGA
XM_011528811.2:c.690+287_690+292delinsCCGCGA XP_011527113.1:n.690+287_690+292delinsCCGCGA
XM_017027841.2:c.690+287_690+292delinsCCGCGA XP_016883330.1:n.690+287_690+292delinsCCGCGA
XM_017027842.2:c.690+287_690+292delinsCCGCGA XP_016883331.1:n.690+287_690+292delinsCCGCGA
XM_017027843.1:c.621+287_621+292delinsCCGCGA XP_016883332.1:n.621+287_621+292delinsCCGCGA
XM_017027844.2:c.690+287_690+292delinsCCGCGA XP_016883333.1:n.690+287_690+292delinsCCGCGA
NM_004518.6:c.690+287_690+292delinsCCGCGA NP_004509.2:n.690+287_690+292delinsCCGCGA
NM_172106.3:c.690+287_690+292delinsCCGCGA NP_742104.1:n.690+287_690+292delinsCCGCGA
NM_172107.4:c.690+287_690+292delinsCCGCGA MANE Select NP_742105.1:n.690+287_690+292delinsCCGCGA
NM_172108.5:c.690+287_690+292delinsCCGCGA NP_742106.1:n.690+287_690+292delinsCCGCGA
NM_172109.3:c.690+287_690+292delinsCCGCGA NP_742107.1:n.690+287_690+292delinsCCGCGA
NM_001382235.1:c.690+287_690+292delinsCCGCGA NP_001369164.1:n.690+287_690+292delinsCCGCGA