Canonical Allele Identifier: CA409638014

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038330G>C (hg19) ; chr20:g.63406977G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406977G>C , CM000682.2:g.63406977G>C	GRCh38
NC_000020.10:g.62038330G>C , CM000682.1:g.62038330G>C	GRCh37
NC_000020.9:g.61508774G>C	NCBI36
NG_009004.1:g.70664C>G
NG_009004.2:g.70664C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2340C>G	ENSP00000516702.1:p.Ser780Arg
ENST00000359125.7:c.2286C>G MANE Select	ENSP00000352035.2:p.Ser762Arg
ENST00000637193.1:c.1683C>G	ENSP00000490734.1:p.Ser561Arg
ENST00000344462.8:c.2193C>G	ENSP00000339611.4:p.Ser731Arg
ENST00000357249.6:c.1854C>G	ENSP00000349789.3:p.Ser618Arg
ENST00000359125.6:c.2286C>G	ENSP00000352035.2:p.Ser762Arg
ENST00000360480.7:c.2202C>G	ENSP00000353668.3:p.Ser734Arg
ENST00000370224.5:c.2241+69C>G	ENSP00000359244.2:n.2241+69C>G
ENST00000625514.2:c.2205+69C>G	ENSP00000486040.1:n.2205+69C>G
ENST00000626839.2:c.2232C>G	ENSP00000486706.1:p.Ser744Arg
ENST00000629241.2:c.2133+69C>G	ENSP00000487142.1:n.2133+69C>G
ENST00000629676.2:c.1680-6134C>G	ENSP00000486194.1:n.1680-6134C>G
NM_004518.4:c.2202C>G	NP_004509.2:p.Ser734Arg
NM_172106.1:c.2232C>G	NP_742104.1:p.Ser744Arg
NM_172107.2:c.2286C>G	NP_742105.1:p.Ser762Arg
NM_172108.3:c.2193C>G	NP_742106.1:p.Ser731Arg
XM_006723787.1:c.2328C>G	XP_006723850.1:p.Ser776Arg
XM_011528807.1:c.2394C>G	XP_011527109.1:p.Ser798Arg
XM_011528808.1:c.2391C>G	XP_011527110.1:p.Ser797Arg
XM_011528809.1:c.2364C>G	XP_011527111.1:p.Ser788Arg
XM_011528810.1:c.2340C>G	XP_011527112.1:p.Ser780Arg
XM_011528811.1:c.2310C>G	XP_011527113.1:p.Ser770Arg
XM_011528812.1:c.2283C>G	XP_011527114.1:p.Ser761Arg
XM_011528813.1:c.2268C>G	XP_011527115.1:p.Ser756Arg
XM_011528814.1:c.1875C>G	XP_011527116.1:p.Ser625Arg
NM_004518.5:c.2202C>G	NP_004509.2:p.Ser734Arg
NM_172106.2:c.2232C>G	NP_742104.1:p.Ser744Arg
NM_172107.3:c.2286C>G	NP_742105.1:p.Ser762Arg
NM_172108.4:c.2193C>G	NP_742106.1:p.Ser731Arg
XM_011528810.2:c.2340C>G	XP_011527112.1:p.Ser780Arg
XM_011528811.2:c.2310C>G	XP_011527113.1:p.Ser770Arg
XM_017027841.2:c.2337C>G	XP_016883330.1:p.Ser779Arg
XM_017027842.2:c.2274C>G	XP_016883331.1:p.Ser758Arg
XM_017027843.1:c.2271C>G	XP_016883332.1:p.Ser757Arg
XM_017027844.2:c.2229C>G	XP_016883333.1:p.Ser743Arg
XM_017027845.1:c.1302C>G	XP_016883334.1:p.Ser434Arg
NM_004518.6:c.2202C>G	NP_004509.2:p.Ser734Arg
NM_172106.3:c.2232C>G	NP_742104.1:p.Ser744Arg
NM_172107.4:c.2286C>G MANE Select	NP_742105.1:p.Ser762Arg
NM_172108.5:c.2193C>G	NP_742106.1:p.Ser731Arg
NM_001382235.1:c.2340C>G	NP_001369164.1:p.Ser780Arg