Canonical Allele Identifier: CA409638077

Gene: KCNQ2

Linked Data

• dbSNP Id: rs2079961921
• gnomAD v4: 20-63406987-T-C
• MyVariant Identifiers: chr20:g.62038340T>C (hg19) ; chr20:g.63406987T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406987T>C , CM000682.2:g.63406987T>C	GRCh38
NC_000020.10:g.62038340T>C , CM000682.1:g.62038340T>C	GRCh37
NC_000020.9:g.61508784T>C	NCBI36
NG_009004.1:g.70654A>G
NG_009004.2:g.70654A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2330A>G	ENSP00000516702.1:p.Asn777Ser
ENST00000359125.7:c.2276A>G MANE Select	ENSP00000352035.2:p.Asn759Ser
ENST00000637193.1:c.1673A>G	ENSP00000490734.1:p.Asn558Ser
ENST00000344462.8:c.2183A>G	ENSP00000339611.4:p.Asn728Ser
ENST00000357249.6:c.1844A>G	ENSP00000349789.3:p.Asn615Ser
ENST00000359125.6:c.2276A>G	ENSP00000352035.2:p.Asn759Ser
ENST00000360480.7:c.2192A>G	ENSP00000353668.3:p.Asn731Ser
ENST00000370224.5:c.2241+59A>G	ENSP00000359244.2:n.2241+59A>G
ENST00000625514.2:c.2205+59A>G	ENSP00000486040.1:n.2205+59A>G
ENST00000626839.2:c.2222A>G	ENSP00000486706.1:p.Asn741Ser
ENST00000629241.2:c.2133+59A>G	ENSP00000487142.1:n.2133+59A>G
ENST00000629676.2:c.1680-6144A>G	ENSP00000486194.1:n.1680-6144A>G
NM_004518.4:c.2192A>G	NP_004509.2:p.Asn731Ser
NM_172106.1:c.2222A>G	NP_742104.1:p.Asn741Ser
NM_172107.2:c.2276A>G	NP_742105.1:p.Asn759Ser
NM_172108.3:c.2183A>G	NP_742106.1:p.Asn728Ser
XM_006723787.1:c.2318A>G	XP_006723850.1:p.Asn773Ser
XM_011528807.1:c.2384A>G	XP_011527109.1:p.Asn795Ser
XM_011528808.1:c.2381A>G	XP_011527110.1:p.Asn794Ser
XM_011528809.1:c.2354A>G	XP_011527111.1:p.Asn785Ser
XM_011528810.1:c.2330A>G	XP_011527112.1:p.Asn777Ser
XM_011528811.1:c.2300A>G	XP_011527113.1:p.Asn767Ser
XM_011528812.1:c.2273A>G	XP_011527114.1:p.Asn758Ser
XM_011528813.1:c.2258A>G	XP_011527115.1:p.Asn753Ser
XM_011528814.1:c.1865A>G	XP_011527116.1:p.Asn622Ser
NM_004518.5:c.2192A>G	NP_004509.2:p.Asn731Ser
NM_172106.2:c.2222A>G	NP_742104.1:p.Asn741Ser
NM_172107.3:c.2276A>G	NP_742105.1:p.Asn759Ser
NM_172108.4:c.2183A>G	NP_742106.1:p.Asn728Ser
XM_011528810.2:c.2330A>G	XP_011527112.1:p.Asn777Ser
XM_011528811.2:c.2300A>G	XP_011527113.1:p.Asn767Ser
XM_017027841.2:c.2327A>G	XP_016883330.1:p.Asn776Ser
XM_017027842.2:c.2264A>G	XP_016883331.1:p.Asn755Ser
XM_017027843.1:c.2261A>G	XP_016883332.1:p.Asn754Ser
XM_017027844.2:c.2219A>G	XP_016883333.1:p.Asn740Ser
XM_017027845.1:c.1292A>G	XP_016883334.1:p.Asn431Ser
NM_004518.6:c.2192A>G	NP_004509.2:p.Asn731Ser
NM_172106.3:c.2222A>G	NP_742104.1:p.Asn741Ser
NM_172107.4:c.2276A>G MANE Select	NP_742105.1:p.Asn759Ser
NM_172108.5:c.2183A>G	NP_742106.1:p.Asn728Ser
NM_001382235.1:c.2330A>G	NP_001369164.1:p.Asn777Ser