Canonical Allele Identifier: CA409639458

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038692T>G (hg19) ; chr20:g.63407339T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407339T>G , CM000682.2:g.63407339T>G	GRCh38
NC_000020.10:g.62038692T>G , CM000682.1:g.62038692T>G	GRCh37
NC_000020.9:g.61509136T>G	NCBI36
NG_009004.1:g.70302A>C
NG_009004.2:g.70302A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1978A>C	ENSP00000516702.1:p.Asn660His
ENST00000359125.7:c.1924A>C MANE Select	ENSP00000352035.2:p.Asn642His
ENST00000637193.1:c.1321A>C	ENSP00000490734.1:p.Asn441His
ENST00000637338.1:n.81A>C
ENST00000344462.8:c.1831A>C	ENSP00000339611.4:p.Asn611His
ENST00000357249.6:c.1492A>C	ENSP00000349789.3:p.Asn498His
ENST00000359125.6:c.1924A>C	ENSP00000352035.2:p.Asn642His
ENST00000360480.7:c.1840A>C	ENSP00000353668.3:p.Asn614His
ENST00000370224.5:c.1948A>C	ENSP00000359244.2:p.Asn650His
ENST00000625514.2:c.1912A>C	ENSP00000486040.1:p.Asn638His
ENST00000626839.2:c.1870A>C	ENSP00000486706.1:p.Asn624His
ENST00000629241.2:c.1840A>C	ENSP00000487142.1:p.Asn614His
ENST00000629676.2:c.1679+6111A>C	ENSP00000486194.1:n.1679+6111A>C
NM_004518.4:c.1840A>C	NP_004509.2:p.Asn614His
NM_172106.1:c.1870A>C	NP_742104.1:p.Asn624His
NM_172107.2:c.1924A>C	NP_742105.1:p.Asn642His
NM_172108.3:c.1831A>C	NP_742106.1:p.Asn611His
XM_006723787.1:c.1966A>C	XP_006723850.1:p.Asn656His
XM_011528807.1:c.2032A>C	XP_011527109.1:p.Asn678His
XM_011528808.1:c.2029A>C	XP_011527110.1:p.Asn677His
XM_011528809.1:c.2002A>C	XP_011527111.1:p.Asn668His
XM_011528810.1:c.1978A>C	XP_011527112.1:p.Asn660His
XM_011528811.1:c.1948A>C	XP_011527113.1:p.Asn650His
XM_011528812.1:c.1921A>C	XP_011527114.1:p.Asn641His
XM_011528813.1:c.1906A>C	XP_011527115.1:p.Asn636His
XM_011528814.1:c.1513A>C	XP_011527116.1:p.Asn505His
NM_004518.5:c.1840A>C	NP_004509.2:p.Asn614His
NM_172106.2:c.1870A>C	NP_742104.1:p.Asn624His
NM_172107.3:c.1924A>C	NP_742105.1:p.Asn642His
NM_172108.4:c.1831A>C	NP_742106.1:p.Asn611His
XM_011528810.2:c.1978A>C	XP_011527112.1:p.Asn660His
XM_011528811.2:c.1948A>C	XP_011527113.1:p.Asn650His
XM_017027841.2:c.1975A>C	XP_016883330.1:p.Asn659His
XM_017027842.2:c.1912A>C	XP_016883331.1:p.Asn638His
XM_017027843.1:c.1909A>C	XP_016883332.1:p.Asn637His
XM_017027844.2:c.1867A>C	XP_016883333.1:p.Asn623His
XM_017027845.1:c.940A>C	XP_016883334.1:p.Asn314His
NM_004518.6:c.1840A>C	NP_004509.2:p.Asn614His
NM_172106.3:c.1870A>C	NP_742104.1:p.Asn624His
NM_172107.4:c.1924A>C MANE Select	NP_742105.1:p.Asn642His
NM_172108.5:c.1831A>C	NP_742106.1:p.Asn611His
NM_001382235.1:c.1978A>C	NP_001369164.1:p.Asn660His