Canonical Allele Identifier: CA409655604

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62076707G>C (hg19) ; chr20:g.63445354G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63445354G>C , CM000682.2:g.63445354G>C	GRCh38
NC_000020.10:g.62076707G>C , CM000682.1:g.62076707G>C	GRCh37
NC_000020.9:g.61547151G>C	NCBI36
NG_009004.1:g.32287C>G
NG_009004.2:g.32287C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.398C>G	ENSP00000516702.1:p.Thr133Ser
ENST00000344425.8:c.398C>G	ENSP00000345523.5:p.Thr133Ser
ENST00000359125.7:c.398C>G MANE Select	ENSP00000352035.2:p.Thr133Ser
ENST00000636255.1:n.136C>G
ENST00000636846.1:n.106C>G
ENST00000637193.1:c.-122C>G	ENSP00000490734.1:n.-122C>G
ENST00000637704.1:n.33C>G
ENST00000344425.7:c.398C>G	ENSP00000345523.5:p.Thr133Ser
ENST00000344462.8:c.398C>G	ENSP00000339611.4:p.Thr133Ser
ENST00000357249.6:c.56C>G	ENSP00000349789.3:p.Thr19Ser
ENST00000359125.6:c.398C>G	ENSP00000352035.2:p.Thr133Ser
ENST00000360480.7:c.398C>G	ENSP00000353668.3:p.Thr133Ser
ENST00000370221.3:n.524C>G
ENST00000370224.5:c.398C>G	ENSP00000359244.2:p.Thr133Ser
ENST00000625514.2:c.398C>G	ENSP00000486040.1:p.Thr133Ser
ENST00000626313.1:n.240C>G
ENST00000626839.2:c.398C>G	ENSP00000486706.1:p.Thr133Ser
ENST00000629241.2:c.398C>G	ENSP00000487142.1:p.Thr133Ser
ENST00000629676.2:c.398C>G	ENSP00000486194.1:p.Thr133Ser
ENST00000630274.2:n.223C>G
NM_004518.4:c.398C>G	NP_004509.2:p.Thr133Ser
NM_172106.1:c.398C>G	NP_742104.1:p.Thr133Ser
NM_172107.2:c.398C>G	NP_742105.1:p.Thr133Ser
NM_172108.3:c.398C>G	NP_742106.1:p.Thr133Ser
NM_172109.1:c.398C>G	NP_742107.1:p.Thr133Ser
XM_006723787.1:c.398C>G	XP_006723850.1:p.Thr133Ser
XM_011528807.1:c.398C>G	XP_011527109.1:p.Thr133Ser
XM_011528808.1:c.398C>G	XP_011527110.1:p.Thr133Ser
XM_011528809.1:c.398C>G	XP_011527111.1:p.Thr133Ser
XM_011528810.1:c.398C>G	XP_011527112.1:p.Thr133Ser
XM_011528811.1:c.398C>G	XP_011527113.1:p.Thr133Ser
XM_011528812.1:c.398C>G	XP_011527114.1:p.Thr133Ser
XM_011528813.1:c.398C>G	XP_011527115.1:p.Thr133Ser
XM_011528814.1:c.-122C>G	XP_011527116.1:n.-122C>G
XM_011528815.1:c.398C>G	XP_011527117.1:p.Thr133Ser
XM_011528816.1:c.398C>G	XP_011527118.1:p.Thr133Ser
NM_004518.5:c.398C>G	NP_004509.2:p.Thr133Ser
NM_172106.2:c.398C>G	NP_742104.1:p.Thr133Ser
NM_172107.3:c.398C>G	NP_742105.1:p.Thr133Ser
NM_172108.4:c.398C>G	NP_742106.1:p.Thr133Ser
NM_172109.2:c.398C>G	NP_742107.1:p.Thr133Ser
XM_011528810.2:c.398C>G	XP_011527112.1:p.Thr133Ser
XM_011528811.2:c.398C>G	XP_011527113.1:p.Thr133Ser
XM_017027841.2:c.398C>G	XP_016883330.1:p.Thr133Ser
XM_017027842.2:c.398C>G	XP_016883331.1:p.Thr133Ser
XM_017027843.1:c.329C>G	XP_016883332.1:p.Thr110Ser
XM_017027844.2:c.398C>G	XP_016883333.1:p.Thr133Ser
NM_004518.6:c.398C>G	NP_004509.2:p.Thr133Ser
NM_172106.3:c.398C>G	NP_742104.1:p.Thr133Ser
NM_172107.4:c.398C>G MANE Select	NP_742105.1:p.Thr133Ser
NM_172108.5:c.398C>G	NP_742106.1:p.Thr133Ser
NM_172109.3:c.398C>G	NP_742107.1:p.Thr133Ser
NM_001382235.1:c.398C>G	NP_001369164.1:p.Thr133Ser