Canonical Allele Identifier: CA9958873
Gene: KCNQ2 HGNC NCBI

Linked Data

dbSNP Id: rs2081443500

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63446883_63446942del , CM000682.2:g.63446883_63446942del GRCh38
NC_000020.10:g.62078236_62078295del , CM000682.1:g.62078236_62078295del GRCh37
NC_000020.9:g.61548680_61548739del NCBI36
NG_009004.1:g.30716_30775del
NG_009004.2:g.30716_30775del

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.297-88_297-29del ENSP00000516702.1:n.297-88_297-29del
ENST00000344425.8:c.297-88_297-29del ENSP00000345523.5:n.297-88_297-29del
ENST00000359125.7:c.297-88_297-29del MANE Select ENSP00000352035.2:n.297-88_297-29del
ENST00000636042.1:n.77-88_77-29del
ENST00000636065.1:n.83-88_83-29del
ENST00000636255.1:n.35-88_35-29del
ENST00000636591.1:n.73-88_73-29del
ENST00000636623.1:n.58-88_58-29del
ENST00000636959.1:n.89-88_89-29del
ENST00000637133.1:n.70-88_70-29del
ENST00000637193.1:c.-223-88_-223-29del ENSP00000490734.1:n.-223-88_-223-29del
ENST00000637772.1:n.30-88_30-29del
ENST00000637803.1:n.95-88_95-29del
ENST00000344425.7:c.297-88_297-29del ENSP00000345523.5:n.297-88_297-29del
ENST00000344462.8:c.297-88_297-29del ENSP00000339611.4:n.297-88_297-29del
ENST00000359125.6:c.297-88_297-29del ENSP00000352035.2:n.297-88_297-29del
ENST00000360480.7:c.297-88_297-29del ENSP00000353668.3:n.297-88_297-29del
ENST00000370221.3:n.423-88_423-29del
ENST00000370224.5:c.297-88_297-29del ENSP00000359244.2:n.297-88_297-29del
ENST00000625514.2:c.297-88_297-29del ENSP00000486040.1:n.297-88_297-29del
ENST00000626313.1:n.139-88_139-29del
ENST00000626839.2:c.297-88_297-29del ENSP00000486706.1:n.297-88_297-29del
ENST00000629241.2:c.297-88_297-29del ENSP00000487142.1:n.297-88_297-29del
ENST00000629676.2:c.297-88_297-29del ENSP00000486194.1:n.297-88_297-29del
NM_004518.4:c.297-88_297-29del NP_004509.2:n.297-88_297-29del
NM_172106.1:c.297-88_297-29del NP_742104.1:n.297-88_297-29del
NM_172107.2:c.297-88_297-29del NP_742105.1:n.297-88_297-29del
NM_172108.3:c.297-88_297-29del NP_742106.1:n.297-88_297-29del
NM_172109.1:c.297-88_297-29del NP_742107.1:n.297-88_297-29del
XM_006723787.1:c.297-88_297-29del XP_006723850.1:n.297-88_297-29del
XM_011528807.1:c.297-88_297-29del XP_011527109.1:n.297-88_297-29del
XM_011528808.1:c.297-88_297-29del XP_011527110.1:n.297-88_297-29del
XM_011528809.1:c.297-88_297-29del XP_011527111.1:n.297-88_297-29del
XM_011528810.1:c.297-88_297-29del XP_011527112.1:n.297-88_297-29del
XM_011528811.1:c.297-88_297-29del XP_011527113.1:n.297-88_297-29del
XM_011528812.1:c.297-88_297-29del XP_011527114.1:n.297-88_297-29del
XM_011528813.1:c.297-88_297-29del XP_011527115.1:n.297-88_297-29del
XM_011528815.1:c.297-88_297-29del XP_011527117.1:n.297-88_297-29del
XM_011528816.1:c.297-88_297-29del XP_011527118.1:n.297-88_297-29del
NM_004518.5:c.297-88_297-29del NP_004509.2:n.297-88_297-29del
NM_172106.2:c.297-88_297-29del NP_742104.1:n.297-88_297-29del
NM_172107.3:c.297-88_297-29del NP_742105.1:n.297-88_297-29del
NM_172108.4:c.297-88_297-29del NP_742106.1:n.297-88_297-29del
NM_172109.2:c.297-88_297-29del NP_742107.1:n.297-88_297-29del
XM_011528810.2:c.297-88_297-29del XP_011527112.1:n.297-88_297-29del
XM_011528811.2:c.297-88_297-29del XP_011527113.1:n.297-88_297-29del
XM_017027841.2:c.297-88_297-29del XP_016883330.1:n.297-88_297-29del
XM_017027842.2:c.297-88_297-29del XP_016883331.1:n.297-88_297-29del
XM_017027843.1:c.228-88_228-29del XP_016883332.1:n.228-88_228-29del
XM_017027844.2:c.297-88_297-29del XP_016883333.1:n.297-88_297-29del
NM_004518.6:c.297-88_297-29del NP_004509.2:n.297-88_297-29del
NM_172106.3:c.297-88_297-29del NP_742104.1:n.297-88_297-29del
NM_172107.4:c.297-88_297-29del MANE Select NP_742105.1:n.297-88_297-29del
NM_172108.5:c.297-88_297-29del NP_742106.1:n.297-88_297-29del
NM_172109.3:c.297-88_297-29del NP_742107.1:n.297-88_297-29del
NM_001382235.1:c.297-88_297-29del NP_001369164.1:n.297-88_297-29del