Canonical Allele Identifier: CA409638952

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 1039210
• ClinVar RCV Id: RCV001342641
• dbSNP Id: rs753033741
• gnomAD v2: 20-62038496-G-A
• gnomAD v3: 20-63407143-G-A
• gnomAD v4: 20-63407143-G-A
• MyVariant Identifiers: chr20:g.62038496G>A (hg19) ; chr20:g.63407143G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407143G>A , CM000682.2:g.63407143G>A	GRCh38
NC_000020.10:g.62038496G>A , CM000682.1:g.62038496G>A	GRCh37
NC_000020.9:g.61508940G>A	NCBI36
NG_009004.1:g.70498C>T
NG_009004.2:g.70498C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2174C>T	ENSP00000516702.1:p.Ala725Val
ENST00000359125.7:c.2120C>T MANE Select	ENSP00000352035.2:p.Ala707Val
ENST00000637193.1:c.1517C>T	ENSP00000490734.1:p.Ala506Val
ENST00000344462.8:c.2027C>T	ENSP00000339611.4:p.Ala676Val
ENST00000357249.6:c.1688C>T	ENSP00000349789.3:p.Ala563Val
ENST00000359125.6:c.2120C>T	ENSP00000352035.2:p.Ala707Val
ENST00000360480.7:c.2036C>T	ENSP00000353668.3:p.Ala679Val
ENST00000370224.5:c.2144C>T	ENSP00000359244.2:p.Ala715Val
ENST00000625514.2:c.2108C>T	ENSP00000486040.1:p.Ala703Val
ENST00000626839.2:c.2066C>T	ENSP00000486706.1:p.Ala689Val
ENST00000629241.2:c.2036C>T	ENSP00000487142.1:p.Ala679Val
ENST00000629676.2:c.1680-6300C>T	ENSP00000486194.1:n.1680-6300C>T
NM_004518.4:c.2036C>T	NP_004509.2:p.Ala679Val
NM_172106.1:c.2066C>T	NP_742104.1:p.Ala689Val
NM_172107.2:c.2120C>T	NP_742105.1:p.Ala707Val
NM_172108.3:c.2027C>T	NP_742106.1:p.Ala676Val
XM_006723787.1:c.2162C>T	XP_006723850.1:p.Ala721Val
XM_011528807.1:c.2228C>T	XP_011527109.1:p.Ala743Val
XM_011528808.1:c.2225C>T	XP_011527110.1:p.Ala742Val
XM_011528809.1:c.2198C>T	XP_011527111.1:p.Ala733Val
XM_011528810.1:c.2174C>T	XP_011527112.1:p.Ala725Val
XM_011528811.1:c.2144C>T	XP_011527113.1:p.Ala715Val
XM_011528812.1:c.2117C>T	XP_011527114.1:p.Ala706Val
XM_011528813.1:c.2102C>T	XP_011527115.1:p.Ala701Val
XM_011528814.1:c.1709C>T	XP_011527116.1:p.Ala570Val
NM_004518.5:c.2036C>T	NP_004509.2:p.Ala679Val
NM_172106.2:c.2066C>T	NP_742104.1:p.Ala689Val
NM_172107.3:c.2120C>T	NP_742105.1:p.Ala707Val
NM_172108.4:c.2027C>T	NP_742106.1:p.Ala676Val
XM_011528810.2:c.2174C>T	XP_011527112.1:p.Ala725Val
XM_011528811.2:c.2144C>T	XP_011527113.1:p.Ala715Val
XM_017027841.2:c.2171C>T	XP_016883330.1:p.Ala724Val
XM_017027842.2:c.2108C>T	XP_016883331.1:p.Ala703Val
XM_017027843.1:c.2105C>T	XP_016883332.1:p.Ala702Val
XM_017027844.2:c.2063C>T	XP_016883333.1:p.Ala688Val
XM_017027845.1:c.1136C>T	XP_016883334.1:p.Ala379Val
NM_004518.6:c.2036C>T	NP_004509.2:p.Ala679Val
NM_172106.3:c.2066C>T	NP_742104.1:p.Ala689Val
NM_172107.4:c.2120C>T MANE Select	NP_742105.1:p.Ala707Val
NM_172108.5:c.2027C>T	NP_742106.1:p.Ala676Val
NM_001382235.1:c.2174C>T	NP_001369164.1:p.Ala725Val