Canonical Allele Identifier: CA511339664

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038705C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407352C>G , CM000682.2:g.63407352C>G	GRCh38
NC_000020.10:g.62038705C>G , CM000682.1:g.62038705C>G	GRCh37
NC_000020.9:g.61509149C>G	NCBI36
NG_009004.1:g.70289G>C
NG_009004.2:g.70289G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1965G>C	ENSP00000516702.1:p.Leu655=
ENST00000359125.7:c.1911G>C MANE Select	ENSP00000352035.2:p.Leu637=
ENST00000637193.1:c.1308G>C	ENSP00000490734.1:p.Leu436=
ENST00000637338.1:n.68G>C
ENST00000344462.8:c.1818G>C	ENSP00000339611.4:p.Leu606=
ENST00000357249.6:c.1479G>C	ENSP00000349789.3:p.Leu493=
ENST00000359125.6:c.1911G>C	ENSP00000352035.2:p.Leu637=
ENST00000360480.7:c.1827G>C	ENSP00000353668.3:p.Leu609=
ENST00000370224.5:c.1935G>C	ENSP00000359244.2:p.Leu645=
ENST00000625514.2:c.1899G>C	ENSP00000486040.1:p.Leu633=
ENST00000626839.2:c.1857G>C	ENSP00000486706.1:p.Leu619=
ENST00000629241.2:c.1827G>C	ENSP00000487142.1:p.Leu609=
ENST00000629676.2:c.1679+6098G>C	ENSP00000486194.1:n.1679+6098G>C
NM_004518.4:c.1827G>C	NP_004509.2:p.Leu609=
NM_172106.1:c.1857G>C	NP_742104.1:p.Leu619=
NM_172107.2:c.1911G>C	NP_742105.1:p.Leu637=
NM_172108.3:c.1818G>C	NP_742106.1:p.Leu606=
XM_006723787.1:c.1953G>C	XP_006723850.1:p.Leu651=
XM_011528807.1:c.2019G>C	XP_011527109.1:p.Leu673=
XM_011528808.1:c.2016G>C	XP_011527110.1:p.Leu672=
XM_011528809.1:c.1989G>C	XP_011527111.1:p.Leu663=
XM_011528810.1:c.1965G>C	XP_011527112.1:p.Leu655=
XM_011528811.1:c.1935G>C	XP_011527113.1:p.Leu645=
XM_011528812.1:c.1908G>C	XP_011527114.1:p.Leu636=
XM_011528813.1:c.1893G>C	XP_011527115.1:p.Leu631=
XM_011528814.1:c.1500G>C	XP_011527116.1:p.Leu500=
NM_004518.5:c.1827G>C	NP_004509.2:p.Leu609=
NM_172106.2:c.1857G>C	NP_742104.1:p.Leu619=
NM_172107.3:c.1911G>C	NP_742105.1:p.Leu637=
NM_172108.4:c.1818G>C	NP_742106.1:p.Leu606=
XM_011528810.2:c.1965G>C	XP_011527112.1:p.Leu655=
XM_011528811.2:c.1935G>C	XP_011527113.1:p.Leu645=
XM_017027841.2:c.1962G>C	XP_016883330.1:p.Leu654=
XM_017027842.2:c.1899G>C	XP_016883331.1:p.Leu633=
XM_017027843.1:c.1896G>C	XP_016883332.1:p.Leu632=
XM_017027844.2:c.1854G>C	XP_016883333.1:p.Leu618=
XM_017027845.1:c.927G>C	XP_016883334.1:p.Leu309=
NM_004518.6:c.1827G>C	NP_004509.2:p.Leu609=
NM_172106.3:c.1857G>C	NP_742104.1:p.Leu619=
NM_172107.4:c.1911G>C MANE Select	NP_742105.1:p.Leu637=
NM_172108.5:c.1818G>C	NP_742106.1:p.Leu606=
NM_001382235.1:c.1965G>C	NP_001369164.1:p.Leu655=