Canonical Allele Identifier: CA342470
Gene: KCNQ2 HGNC NCBI

Linked Data

ClinVar Variation Id: 21763
dbSNP Id: rs118192228

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63414902C>T , CM000682.2:g.63414902C>T GRCh38
NC_000020.10:g.62046255C>T , CM000682.1:g.62046255C>T GRCh37
NC_000020.9:g.61516699C>T NCBI36
NG_009004.1:g.62739G>A
NG_009004.2:g.62739G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706989.1:c.1471+1G>A ENSP00000516702.1:n.1471+1G>A
ENST00000359125.7:c.1525+1G>A MANE Select ENSP00000352035.2:n.1525+1G>A
ENST00000637193.1:c.922+1G>A ENSP00000490734.1:n.922+1G>A
ENST00000344462.8:c.1435+1G>A ENSP00000339611.4:n.1435+1G>A
ENST00000357249.6:c.1093+1G>A ENSP00000349789.3:n.1093+1G>A
ENST00000359125.6:c.1525+1G>A ENSP00000352035.2:n.1525+1G>A
ENST00000360480.7:c.1441+1G>A ENSP00000353668.3:n.1441+1G>A
ENST00000370224.5:c.1441+1G>A ENSP00000359244.2:n.1441+1G>A
ENST00000625514.2:c.1405+1G>A ENSP00000486040.1:n.1405+1G>A
ENST00000626839.2:c.1471+1G>A ENSP00000486706.1:n.1471+1G>A
ENST00000627221.2:c.585+1G>A
ENST00000629241.2:c.1441+1G>A ENSP00000487142.1:n.1441+1G>A
ENST00000629318.1:c.133+1G>A ENSP00000487384.1:n.133+1G>A
ENST00000629676.2:c.1441+1G>A ENSP00000486194.1:n.1441+1G>A
NM_004518.4:c.1441+1G>A NP_004509.2:n.1441+1G>A
NM_172106.1:c.1471+1G>A NP_742104.1:n.1471+1G>A
NM_172107.2:c.1525+1G>A NP_742105.1:n.1525+1G>A
NM_172108.3:c.1435+1G>A NP_742106.1:n.1435+1G>A
XM_006723787.1:c.1525+1G>A XP_006723850.1:n.1525+1G>A
XM_011528807.1:c.1525+1G>A XP_011527109.1:n.1525+1G>A
XM_011528808.1:c.1525+1G>A XP_011527110.1:n.1525+1G>A
XM_011528809.1:c.1495+1G>A XP_011527111.1:n.1495+1G>A
XM_011528810.1:c.1471+1G>A XP_011527112.1:n.1471+1G>A
XM_011528811.1:c.1441+1G>A XP_011527113.1:n.1441+1G>A
XM_011528812.1:c.1525+1G>A XP_011527114.1:n.1525+1G>A
XM_011528813.1:c.1399+1G>A XP_011527115.1:n.1399+1G>A
XM_011528814.1:c.1006+1G>A XP_011527116.1:n.1006+1G>A
XM_011528815.1:c.1525+1G>A XP_011527117.1:n.1525+1G>A
NM_004518.5:c.1441+1G>A NP_004509.2:n.1441+1G>A
NM_172106.2:c.1471+1G>A NP_742104.1:n.1471+1G>A
NM_172107.3:c.1525+1G>A NP_742105.1:n.1525+1G>A
NM_172108.4:c.1435+1G>A NP_742106.1:n.1435+1G>A
XM_011528810.2:c.1471+1G>A XP_011527112.1:n.1471+1G>A
XM_011528811.2:c.1441+1G>A XP_011527113.1:n.1441+1G>A
XM_017027841.2:c.1471+1G>A XP_016883330.1:n.1471+1G>A
XM_017027842.2:c.1471+1G>A XP_016883331.1:n.1471+1G>A
XM_017027843.1:c.1402+1G>A XP_016883332.1:n.1402+1G>A
XM_017027844.2:c.1471+1G>A XP_016883333.1:n.1471+1G>A
XM_017027845.1:c.433+1G>A XP_016883334.1:n.433+1G>A
NM_004518.6:c.1441+1G>A NP_004509.2:n.1441+1G>A
NM_172106.3:c.1471+1G>A NP_742104.1:n.1471+1G>A
NM_172107.4:c.1525+1G>A MANE Select NP_742105.1:n.1525+1G>A
NM_172108.5:c.1435+1G>A NP_742106.1:n.1435+1G>A
NM_001382235.1:c.1471+1G>A NP_001369164.1:n.1471+1G>A