Canonical Allele Identifier: CA2374785536
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63428302_63428314delinsGGGCAGCTGGGGC , CM000682.2:g.63428302_63428314delinsGGGCAGCTGGGGC GRCh38
NC_000020.10:g.62059655_62059667delinsGGGCAGCTGGGGC , CM000682.1:g.62059655_62059667delinsGGGCAGCTGGGGC GRCh37
NC_000020.9:g.61530099_61530111delinsGGGCAGCTGGGGC NCBI36
NG_009004.1:g.49327_49339delinsGCCCCAGCTGCCC
NG_009004.2:g.49327_49339delinsGCCCCAGCTGCCC

Transcript Alleles

HGVS Amino-acid change
ENST00000706989.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC ENSP00000516702.1:n.1217+53_1217+65delins...
ENST00000359125.7:c.1217+53_1217+65delinsGCCCCAGCTGCCC MANE Select ENSP00000352035.2:n.1217+53_1217+65delins...
ENST00000637193.1:c.668+53_668+65delinsGCCCCAGCTGCCC ENSP00000490734.1:n.668+53_668+65delinsGC...
ENST00000637632.1:n.56+53_56+65delinsGCCCCAGCTGCCC
ENST00000344462.8:c.1217+53_1217+65delinsGCCCCAGCTGCCC ENSP00000339611.4:n.1217+53_1217+65delins...
ENST00000357249.6:c.875+53_875+65delinsGCCCCAGCTGCCC ENSP00000349789.3:n.875+53_875+65delinsGC...
ENST00000359125.6:c.1217+53_1217+65delinsGCCCCAGCTGCCC ENSP00000352035.2:n.1217+53_1217+65delins...
ENST00000360480.7:c.1187+53_1187+65delinsGCCCCAGCTGCCC ENSP00000353668.3:n.1187+53_1187+65delins...
ENST00000370221.3:n.1343+53_1343+65delinsGCCCCAGCTGCCC
ENST00000370224.5:c.1187+53_1187+65delinsGCCCCAGCTGCCC ENSP00000359244.2:n.1187+53_1187+65delins...
ENST00000625514.2:c.1187+53_1187+65delinsGCCCCAGCTGCCC ENSP00000486040.1:n.1187+53_1187+65delins...
ENST00000626839.2:c.1217+53_1217+65delinsGCCCCAGCTGCCC ENSP00000486706.1:n.1217+53_1217+65delins...
ENST00000627221.2:c.331+53_331+65delinsGCCCCAGCTGCCC
ENST00000629241.2:c.1187+53_1187+65delinsGCCCCAGCTGCCC ENSP00000487142.1:n.1187+53_1187+65delins...
ENST00000629676.2:c.1187+53_1187+65delinsGCCCCAGCTGCCC ENSP00000486194.1:n.1187+53_1187+65delins...
NM_004518.4:c.1187+53_1187+65delinsGCCCCAGCTGCCC NP_004509.2:n.1187+53_1187+65delinsGCCCCA...
NM_172106.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742104.1:n.1217+53_1217+65delinsGCCCCA...
NM_172107.2:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742105.1:n.1217+53_1217+65delinsGCCCCA...
NM_172108.3:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742106.1:n.1217+53_1217+65delinsGCCCCA...
XM_006723787.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_006723850.1:n.1217+53_1217+65delinsGCC...
XM_011528807.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_011527109.1:n.1217+53_1217+65delinsGCC...
XM_011528808.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_011527110.1:n.1217+53_1217+65delinsGCC...
XM_011528809.1:c.1187+53_1187+65delinsGCCCCAGCTGCCC XP_011527111.1:n.1187+53_1187+65delinsGCC...
XM_011528810.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_011527112.1:n.1217+53_1217+65delinsGCC...
XM_011528811.1:c.1187+53_1187+65delinsGCCCCAGCTGCCC XP_011527113.1:n.1187+53_1187+65delinsGCC...
XM_011528812.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_011527114.1:n.1217+53_1217+65delinsGCC...
XM_011528813.1:c.1091+53_1091+65delinsGCCCCAGCTGCCC XP_011527115.1:n.1091+53_1091+65delinsGCC...
XM_011528814.1:c.698+53_698+65delinsGCCCCAGCTGCCC XP_011527116.1:n.698+53_698+65delinsGCCCC...
XM_011528815.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_011527117.1:n.1217+53_1217+65delinsGCC...
NM_004518.5:c.1187+53_1187+65delinsGCCCCAGCTGCCC NP_004509.2:n.1187+53_1187+65delinsGCCCCA...
NM_172106.2:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742104.1:n.1217+53_1217+65delinsGCCCCA...
NM_172107.3:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742105.1:n.1217+53_1217+65delinsGCCCCA...
NM_172108.4:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742106.1:n.1217+53_1217+65delinsGCCCCA...
XM_011528810.2:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_011527112.1:n.1217+53_1217+65delinsGCC...
XM_011528811.2:c.1187+53_1187+65delinsGCCCCAGCTGCCC XP_011527113.1:n.1187+53_1187+65delinsGCC...
XM_017027841.2:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_016883330.1:n.1217+53_1217+65delinsGCC...
XM_017027842.2:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_016883331.1:n.1217+53_1217+65delinsGCC...
XM_017027843.1:c.1148+53_1148+65delinsGCCCCAGCTGCCC XP_016883332.1:n.1148+53_1148+65delinsGCC...
XM_017027844.2:c.1217+53_1217+65delinsGCCCCAGCTGCCC XP_016883333.1:n.1217+53_1217+65delinsGCC...
NM_004518.6:c.1187+53_1187+65delinsGCCCCAGCTGCCC NP_004509.2:n.1187+53_1187+65delinsGCCCCA...
NM_172106.3:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742104.1:n.1217+53_1217+65delinsGCCCCA...
NM_172107.4:c.1217+53_1217+65delinsGCCCCAGCTGCCC MANE Select NP_742105.1:n.1217+53_1217+65delinsGCCCCA...
NM_172108.5:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_742106.1:n.1217+53_1217+65delinsGCCCCA...
NM_001382235.1:c.1217+53_1217+65delinsGCCCCAGCTGCCC NP_001369164.1:n.1217+53_1217+65delinsGCC...