Canonical Allele Identifier: CA2736827450
Gene: KCNQ2 HGNC NCBI

Linked Data

dbSNP Id: rs745798144

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63415157_63415158insCACACAGA , CM000682.2:g.63415157_63415158insCACACAGA GRCh38
NC_000020.10:g.62046510_62046511insCACACAGA , CM000682.1:g.62046510_62046511insCACACAGA GRCh37
NC_000020.9:g.61516954_61516955insCACACAGA NCBI36
NG_009004.1:g.62488_62489insGTGTCTGT
NG_009004.2:g.62488_62489insGTGTCTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000706989.1:c.1248-27_1248-26insGTGTCTGT ENSP00000516702.1:n.1248-27_1248-26insGTGTCTGT
ENST00000359125.7:c.1302-27_1302-26insGTGTCTGT MANE Select ENSP00000352035.2:n.1302-27_1302-26insGTGTCTGT
ENST00000637193.1:c.699-27_699-26insGTGTCTGT ENSP00000490734.1:n.699-27_699-26insGTGTCTGT
ENST00000637584.1:n.75-63_75-62insGTGTCTGT
ENST00000344462.8:c.1248-63_1248-62insGTGTCTGT ENSP00000339611.4:n.1248-63_1248-62insGTGTCTGT
ENST00000357249.6:c.906-63_906-62insGTGTCTGT ENSP00000349789.3:n.906-63_906-62insGTGTCTGT
ENST00000359125.6:c.1302-27_1302-26insGTGTCTGT ENSP00000352035.2:n.1302-27_1302-26insGTGTCTGT
ENST00000360480.7:c.1218-27_1218-26insGTGTCTGT ENSP00000353668.3:n.1218-27_1218-26insGTGTCTGT
ENST00000370224.5:c.1218-27_1218-26insGTGTCTGT ENSP00000359244.2:n.1218-27_1218-26insGTGTCTGT
ENST00000625514.2:c.1218-63_1218-62insGTGTCTGT ENSP00000486040.1:n.1218-63_1218-62insGTGTCTGT
ENST00000626839.2:c.1248-27_1248-26insGTGTCTGT ENSP00000486706.1:n.1248-27_1248-26insGTGTCTGT
ENST00000627221.2:c.362-27_362-26insGTGTCTGT
ENST00000629241.2:c.1218-27_1218-26insGTGTCTGT ENSP00000487142.1:n.1218-27_1218-26insGTGTCTGT
ENST00000629676.2:c.1218-27_1218-26insGTGTCTGT ENSP00000486194.1:n.1218-27_1218-26insGTGTCTGT
NM_004518.4:c.1218-27_1218-26insGTGTCTGT NP_004509.2:n.1218-27_1218-26insGTGTCTGT
NM_172106.1:c.1248-27_1248-26insGTGTCTGT NP_742104.1:n.1248-27_1248-26insGTGTCTGT
NM_172107.2:c.1302-27_1302-26insGTGTCTGT NP_742105.1:n.1302-27_1302-26insGTGTCTGT
NM_172108.3:c.1248-63_1248-62insGTGTCTGT NP_742106.1:n.1248-63_1248-62insGTGTCTGT
XM_006723787.1:c.1302-27_1302-26insGTGTCTGT XP_006723850.1:n.1302-27_1302-26insGTGTCTGT
XM_011528807.1:c.1302-27_1302-26insGTGTCTGT XP_011527109.1:n.1302-27_1302-26insGTGTCTGT
XM_011528808.1:c.1302-27_1302-26insGTGTCTGT XP_011527110.1:n.1302-27_1302-26insGTGTCTGT
XM_011528809.1:c.1272-27_1272-26insGTGTCTGT XP_011527111.1:n.1272-27_1272-26insGTGTCTGT
XM_011528810.1:c.1248-27_1248-26insGTGTCTGT XP_011527112.1:n.1248-27_1248-26insGTGTCTGT
XM_011528811.1:c.1218-27_1218-26insGTGTCTGT XP_011527113.1:n.1218-27_1218-26insGTGTCTGT
XM_011528812.1:c.1302-27_1302-26insGTGTCTGT XP_011527114.1:n.1302-27_1302-26insGTGTCTGT
XM_011528813.1:c.1176-27_1176-26insGTGTCTGT XP_011527115.1:n.1176-27_1176-26insGTGTCTGT
XM_011528814.1:c.783-27_783-26insGTGTCTGT XP_011527116.1:n.783-27_783-26insGTGTCTGT
XM_011528815.1:c.1302-27_1302-26insGTGTCTGT XP_011527117.1:n.1302-27_1302-26insGTGTCTGT
NM_004518.5:c.1218-27_1218-26insGTGTCTGT NP_004509.2:n.1218-27_1218-26insGTGTCTGT
NM_172106.2:c.1248-27_1248-26insGTGTCTGT NP_742104.1:n.1248-27_1248-26insGTGTCTGT
NM_172107.3:c.1302-27_1302-26insGTGTCTGT NP_742105.1:n.1302-27_1302-26insGTGTCTGT
NM_172108.4:c.1248-63_1248-62insGTGTCTGT NP_742106.1:n.1248-63_1248-62insGTGTCTGT
XM_011528810.2:c.1248-27_1248-26insGTGTCTGT XP_011527112.1:n.1248-27_1248-26insGTGTCTGT
XM_011528811.2:c.1218-27_1218-26insGTGTCTGT XP_011527113.1:n.1218-27_1218-26insGTGTCTGT
XM_017027841.2:c.1248-27_1248-26insGTGTCTGT XP_016883330.1:n.1248-27_1248-26insGTGTCTGT
XM_017027842.2:c.1248-27_1248-26insGTGTCTGT XP_016883331.1:n.1248-27_1248-26insGTGTCTGT
XM_017027843.1:c.1179-27_1179-26insGTGTCTGT XP_016883332.1:n.1179-27_1179-26insGTGTCTGT
XM_017027844.2:c.1248-27_1248-26insGTGTCTGT XP_016883333.1:n.1248-27_1248-26insGTGTCTGT
XM_017027845.1:c.210-27_210-26insGTGTCTGT XP_016883334.1:n.210-27_210-26insGTGTCTGT
NM_004518.6:c.1218-27_1218-26insGTGTCTGT NP_004509.2:n.1218-27_1218-26insGTGTCTGT
NM_172106.3:c.1248-27_1248-26insGTGTCTGT NP_742104.1:n.1248-27_1248-26insGTGTCTGT
NM_172107.4:c.1302-27_1302-26insGTGTCTGT MANE Select NP_742105.1:n.1302-27_1302-26insGTGTCTGT
NM_172108.5:c.1248-63_1248-62insGTGTCTGT NP_742106.1:n.1248-63_1248-62insGTGTCTGT
NM_001382235.1:c.1248-27_1248-26insGTGTCTGT NP_001369164.1:n.1248-27_1248-26insGTGTCTGT