Canonical Allele Identifier: CA511339572

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038669G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407316G>C , CM000682.2:g.63407316G>C	GRCh38
NC_000020.10:g.62038669G>C , CM000682.1:g.62038669G>C	GRCh37
NC_000020.9:g.61509113G>C	NCBI36
NG_009004.1:g.70325C>G
NG_009004.2:g.70325C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2001C>G	ENSP00000516702.1:p.Gly667=
ENST00000359125.7:c.1947C>G MANE Select	ENSP00000352035.2:p.Gly649=
ENST00000637193.1:c.1344C>G	ENSP00000490734.1:p.Gly448=
ENST00000344462.8:c.1854C>G	ENSP00000339611.4:p.Gly618=
ENST00000357249.6:c.1515C>G	ENSP00000349789.3:p.Gly505=
ENST00000359125.6:c.1947C>G	ENSP00000352035.2:p.Gly649=
ENST00000360480.7:c.1863C>G	ENSP00000353668.3:p.Gly621=
ENST00000370224.5:c.1971C>G	ENSP00000359244.2:p.Gly657=
ENST00000625514.2:c.1935C>G	ENSP00000486040.1:p.Gly645=
ENST00000626839.2:c.1893C>G	ENSP00000486706.1:p.Gly631=
ENST00000629241.2:c.1863C>G	ENSP00000487142.1:p.Gly621=
ENST00000629676.2:c.1679+6134C>G	ENSP00000486194.1:n.1679+6134C>G
NM_004518.4:c.1863C>G	NP_004509.2:p.Gly621=
NM_172106.1:c.1893C>G	NP_742104.1:p.Gly631=
NM_172107.2:c.1947C>G	NP_742105.1:p.Gly649=
NM_172108.3:c.1854C>G	NP_742106.1:p.Gly618=
XM_006723787.1:c.1989C>G	XP_006723850.1:p.Gly663=
XM_011528807.1:c.2055C>G	XP_011527109.1:p.Gly685=
XM_011528808.1:c.2052C>G	XP_011527110.1:p.Gly684=
XM_011528809.1:c.2025C>G	XP_011527111.1:p.Gly675=
XM_011528810.1:c.2001C>G	XP_011527112.1:p.Gly667=
XM_011528811.1:c.1971C>G	XP_011527113.1:p.Gly657=
XM_011528812.1:c.1944C>G	XP_011527114.1:p.Gly648=
XM_011528813.1:c.1929C>G	XP_011527115.1:p.Gly643=
XM_011528814.1:c.1536C>G	XP_011527116.1:p.Gly512=
NM_004518.5:c.1863C>G	NP_004509.2:p.Gly621=
NM_172106.2:c.1893C>G	NP_742104.1:p.Gly631=
NM_172107.3:c.1947C>G	NP_742105.1:p.Gly649=
NM_172108.4:c.1854C>G	NP_742106.1:p.Gly618=
XM_011528810.2:c.2001C>G	XP_011527112.1:p.Gly667=
XM_011528811.2:c.1971C>G	XP_011527113.1:p.Gly657=
XM_017027841.2:c.1998C>G	XP_016883330.1:p.Gly666=
XM_017027842.2:c.1935C>G	XP_016883331.1:p.Gly645=
XM_017027843.1:c.1932C>G	XP_016883332.1:p.Gly644=
XM_017027844.2:c.1890C>G	XP_016883333.1:p.Gly630=
XM_017027845.1:c.963C>G	XP_016883334.1:p.Gly321=
NM_004518.6:c.1863C>G	NP_004509.2:p.Gly621=
NM_172106.3:c.1893C>G	NP_742104.1:p.Gly631=
NM_172107.4:c.1947C>G MANE Select	NP_742105.1:p.Gly649=
NM_172108.5:c.1854C>G	NP_742106.1:p.Gly618=
NM_001382235.1:c.2001C>G	NP_001369164.1:p.Gly667=