Canonical Allele Identifier: CA409646650

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 2885386
• ClinVar RCV Id: RCV003752932
• dbSNP Id: rs2145556369
• MyVariant Identifiers: chr20:g.62046372T>C (hg19) ; chr20:g.63415019T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63415019T>C , CM000682.2:g.63415019T>C	GRCh38
NC_000020.10:g.62046372T>C , CM000682.1:g.62046372T>C	GRCh37
NC_000020.9:g.61516816T>C	NCBI36
NG_009004.1:g.62622A>G
NG_009004.2:g.62622A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706989.1:c.1355A>G	ENSP00000516702.1:p.Asp452Gly
ENST00000359125.7:c.1409A>G MANE Select	ENSP00000352035.2:p.Asp470Gly
ENST00000637193.1:c.806A>G	ENSP00000490734.1:p.Asp269Gly
ENST00000344462.8:c.1319A>G	ENSP00000339611.4:p.Asp440Gly
ENST00000357249.6:c.977A>G	ENSP00000349789.3:p.Asp326Gly
ENST00000359125.6:c.1409A>G	ENSP00000352035.2:p.Asp470Gly
ENST00000360480.7:c.1325A>G	ENSP00000353668.3:p.Asp442Gly
ENST00000370224.5:c.1325A>G	ENSP00000359244.2:p.Asp442Gly
ENST00000625514.2:c.1289A>G	ENSP00000486040.1:p.Asp430Gly
ENST00000626839.2:c.1355A>G	ENSP00000486706.1:p.Asp452Gly
ENST00000627221.2:c.469A>G
ENST00000629241.2:c.1325A>G	ENSP00000487142.1:p.Asp442Gly
ENST00000629318.1:c.17A>G	ENSP00000487384.1:p.Asp6Gly
ENST00000629676.2:c.1325A>G	ENSP00000486194.1:p.Asp442Gly
NM_004518.4:c.1325A>G	NP_004509.2:p.Asp442Gly
NM_172106.1:c.1355A>G	NP_742104.1:p.Asp452Gly
NM_172107.2:c.1409A>G	NP_742105.1:p.Asp470Gly
NM_172108.3:c.1319A>G	NP_742106.1:p.Asp440Gly
XM_006723787.1:c.1409A>G	XP_006723850.1:p.Asp470Gly
XM_011528807.1:c.1409A>G	XP_011527109.1:p.Asp470Gly
XM_011528808.1:c.1409A>G	XP_011527110.1:p.Asp470Gly
XM_011528809.1:c.1379A>G	XP_011527111.1:p.Asp460Gly
XM_011528810.1:c.1355A>G	XP_011527112.1:p.Asp452Gly
XM_011528811.1:c.1325A>G	XP_011527113.1:p.Asp442Gly
XM_011528812.1:c.1409A>G	XP_011527114.1:p.Asp470Gly
XM_011528813.1:c.1283A>G	XP_011527115.1:p.Asp428Gly
XM_011528814.1:c.890A>G	XP_011527116.1:p.Asp297Gly
XM_011528815.1:c.1409A>G	XP_011527117.1:p.Asp470Gly
NM_004518.5:c.1325A>G	NP_004509.2:p.Asp442Gly
NM_172106.2:c.1355A>G	NP_742104.1:p.Asp452Gly
NM_172107.3:c.1409A>G	NP_742105.1:p.Asp470Gly
NM_172108.4:c.1319A>G	NP_742106.1:p.Asp440Gly
XM_011528810.2:c.1355A>G	XP_011527112.1:p.Asp452Gly
XM_011528811.2:c.1325A>G	XP_011527113.1:p.Asp442Gly
XM_017027841.2:c.1355A>G	XP_016883330.1:p.Asp452Gly
XM_017027842.2:c.1355A>G	XP_016883331.1:p.Asp452Gly
XM_017027843.1:c.1286A>G	XP_016883332.1:p.Asp429Gly
XM_017027844.2:c.1355A>G	XP_016883333.1:p.Asp452Gly
XM_017027845.1:c.317A>G	XP_016883334.1:p.Asp106Gly
NM_004518.6:c.1325A>G	NP_004509.2:p.Asp442Gly
NM_172106.3:c.1355A>G	NP_742104.1:p.Asp452Gly
NM_172107.4:c.1409A>G MANE Select	NP_742105.1:p.Asp470Gly
NM_172108.5:c.1319A>G	NP_742106.1:p.Asp440Gly
NM_001382235.1:c.1355A>G	NP_001369164.1:p.Asp452Gly