Canonical Allele Identifier: CA2374778989
Gene: KCNQ2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63415318_63415319delinsGA , CM000682.2:g.63415318_63415319delinsGA GRCh38
NC_000020.10:g.62046671_62046672delinsGA , CM000682.1:g.62046671_62046672delinsGA GRCh37
NC_000020.9:g.61517115_61517116delinsGA NCBI36
NG_009004.1:g.62322_62323delinsTC
NG_009004.2:g.62322_62323delinsTC

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.1248-193_1248-192delinsTC ENSP00000516702.1:n.1248-193_1248-192delinsTC
ENST00000359125.7:c.1302-193_1302-192delinsTC MANE Select ENSP00000352035.2:n.1302-193_1302-192delinsTC
ENST00000637193.1:c.699-193_699-192delinsTC ENSP00000490734.1:n.699-193_699-192delinsTC
ENST00000637584.1:n.75-229_75-228delinsTC
ENST00000344462.8:c.1248-229_1248-228delinsTC ENSP00000339611.4:n.1248-229_1248-228delinsTC
ENST00000357249.6:c.906-229_906-228delinsTC ENSP00000349789.3:n.906-229_906-228delinsTC
ENST00000359125.6:c.1302-193_1302-192delinsTC ENSP00000352035.2:n.1302-193_1302-192delinsTC
ENST00000360480.7:c.1218-193_1218-192delinsTC ENSP00000353668.3:n.1218-193_1218-192delinsTC
ENST00000370224.5:c.1218-193_1218-192delinsTC ENSP00000359244.2:n.1218-193_1218-192delinsTC
ENST00000625514.2:c.1218-229_1218-228delinsTC ENSP00000486040.1:n.1218-229_1218-228delinsTC
ENST00000626839.2:c.1248-193_1248-192delinsTC ENSP00000486706.1:n.1248-193_1248-192delinsTC
ENST00000627221.2:c.362-193_362-192delinsTC
ENST00000629241.2:c.1218-193_1218-192delinsTC ENSP00000487142.1:n.1218-193_1218-192delinsTC
ENST00000629676.2:c.1218-193_1218-192delinsTC ENSP00000486194.1:n.1218-193_1218-192delinsTC
NM_004518.4:c.1218-193_1218-192delinsTC NP_004509.2:n.1218-193_1218-192delinsTC
NM_172106.1:c.1248-193_1248-192delinsTC NP_742104.1:n.1248-193_1248-192delinsTC
NM_172107.2:c.1302-193_1302-192delinsTC NP_742105.1:n.1302-193_1302-192delinsTC
NM_172108.3:c.1248-229_1248-228delinsTC NP_742106.1:n.1248-229_1248-228delinsTC
XM_006723787.1:c.1302-193_1302-192delinsTC XP_006723850.1:n.1302-193_1302-192delinsTC
XM_011528807.1:c.1302-193_1302-192delinsTC XP_011527109.1:n.1302-193_1302-192delinsTC
XM_011528808.1:c.1302-193_1302-192delinsTC XP_011527110.1:n.1302-193_1302-192delinsTC
XM_011528809.1:c.1272-193_1272-192delinsTC XP_011527111.1:n.1272-193_1272-192delinsTC
XM_011528810.1:c.1248-193_1248-192delinsTC XP_011527112.1:n.1248-193_1248-192delinsTC
XM_011528811.1:c.1218-193_1218-192delinsTC XP_011527113.1:n.1218-193_1218-192delinsTC
XM_011528812.1:c.1302-193_1302-192delinsTC XP_011527114.1:n.1302-193_1302-192delinsTC
XM_011528813.1:c.1176-193_1176-192delinsTC XP_011527115.1:n.1176-193_1176-192delinsTC
XM_011528814.1:c.783-193_783-192delinsTC XP_011527116.1:n.783-193_783-192delinsTC
XM_011528815.1:c.1302-193_1302-192delinsTC XP_011527117.1:n.1302-193_1302-192delinsTC
NM_004518.5:c.1218-193_1218-192delinsTC NP_004509.2:n.1218-193_1218-192delinsTC
NM_172106.2:c.1248-193_1248-192delinsTC NP_742104.1:n.1248-193_1248-192delinsTC
NM_172107.3:c.1302-193_1302-192delinsTC NP_742105.1:n.1302-193_1302-192delinsTC
NM_172108.4:c.1248-229_1248-228delinsTC NP_742106.1:n.1248-229_1248-228delinsTC
XM_011528810.2:c.1248-193_1248-192delinsTC XP_011527112.1:n.1248-193_1248-192delinsTC
XM_011528811.2:c.1218-193_1218-192delinsTC XP_011527113.1:n.1218-193_1218-192delinsTC
XM_017027841.2:c.1248-193_1248-192delinsTC XP_016883330.1:n.1248-193_1248-192delinsTC
XM_017027842.2:c.1248-193_1248-192delinsTC XP_016883331.1:n.1248-193_1248-192delinsTC
XM_017027843.1:c.1179-193_1179-192delinsTC XP_016883332.1:n.1179-193_1179-192delinsTC
XM_017027844.2:c.1248-193_1248-192delinsTC XP_016883333.1:n.1248-193_1248-192delinsTC
XM_017027845.1:c.210-193_210-192delinsTC XP_016883334.1:n.210-193_210-192delinsTC
NM_004518.6:c.1218-193_1218-192delinsTC NP_004509.2:n.1218-193_1218-192delinsTC
NM_172106.3:c.1248-193_1248-192delinsTC NP_742104.1:n.1248-193_1248-192delinsTC
NM_172107.4:c.1302-193_1302-192delinsTC MANE Select NP_742105.1:n.1302-193_1302-192delinsTC
NM_172108.5:c.1248-229_1248-228delinsTC NP_742106.1:n.1248-229_1248-228delinsTC
NM_001382235.1:c.1248-193_1248-192delinsTC NP_001369164.1:n.1248-193_1248-192delinsTC