Canonical Allele Identifier: CA409639550

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038712T>C (hg19) ; chr20:g.63407359T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407359T>C , CM000682.2:g.63407359T>C	GRCh38
NC_000020.10:g.62038712T>C , CM000682.1:g.62038712T>C	GRCh37
NC_000020.9:g.61509156T>C	NCBI36
NG_009004.1:g.70282A>G
NG_009004.2:g.70282A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1958A>G	ENSP00000516702.1:p.Lys653Arg
ENST00000359125.7:c.1904A>G MANE Select	ENSP00000352035.2:p.Lys635Arg
ENST00000637193.1:c.1301A>G	ENSP00000490734.1:p.Lys434Arg
ENST00000637338.1:n.61A>G
ENST00000344462.8:c.1811A>G	ENSP00000339611.4:p.Lys604Arg
ENST00000357249.6:c.1472A>G	ENSP00000349789.3:p.Lys491Arg
ENST00000359125.6:c.1904A>G	ENSP00000352035.2:p.Lys635Arg
ENST00000360480.7:c.1820A>G	ENSP00000353668.3:p.Lys607Arg
ENST00000370224.5:c.1928A>G	ENSP00000359244.2:p.Lys643Arg
ENST00000625514.2:c.1892A>G	ENSP00000486040.1:p.Lys631Arg
ENST00000626839.2:c.1850A>G	ENSP00000486706.1:p.Lys617Arg
ENST00000629241.2:c.1820A>G	ENSP00000487142.1:p.Lys607Arg
ENST00000629676.2:c.1679+6091A>G	ENSP00000486194.1:n.1679+6091A>G
NM_004518.4:c.1820A>G	NP_004509.2:p.Lys607Arg
NM_172106.1:c.1850A>G	NP_742104.1:p.Lys617Arg
NM_172107.2:c.1904A>G	NP_742105.1:p.Lys635Arg
NM_172108.3:c.1811A>G	NP_742106.1:p.Lys604Arg
XM_006723787.1:c.1946A>G	XP_006723850.1:p.Lys649Arg
XM_011528807.1:c.2012A>G	XP_011527109.1:p.Lys671Arg
XM_011528808.1:c.2009A>G	XP_011527110.1:p.Lys670Arg
XM_011528809.1:c.1982A>G	XP_011527111.1:p.Lys661Arg
XM_011528810.1:c.1958A>G	XP_011527112.1:p.Lys653Arg
XM_011528811.1:c.1928A>G	XP_011527113.1:p.Lys643Arg
XM_011528812.1:c.1901A>G	XP_011527114.1:p.Lys634Arg
XM_011528813.1:c.1886A>G	XP_011527115.1:p.Lys629Arg
XM_011528814.1:c.1493A>G	XP_011527116.1:p.Lys498Arg
NM_004518.5:c.1820A>G	NP_004509.2:p.Lys607Arg
NM_172106.2:c.1850A>G	NP_742104.1:p.Lys617Arg
NM_172107.3:c.1904A>G	NP_742105.1:p.Lys635Arg
NM_172108.4:c.1811A>G	NP_742106.1:p.Lys604Arg
XM_011528810.2:c.1958A>G	XP_011527112.1:p.Lys653Arg
XM_011528811.2:c.1928A>G	XP_011527113.1:p.Lys643Arg
XM_017027841.2:c.1955A>G	XP_016883330.1:p.Lys652Arg
XM_017027842.2:c.1892A>G	XP_016883331.1:p.Lys631Arg
XM_017027843.1:c.1889A>G	XP_016883332.1:p.Lys630Arg
XM_017027844.2:c.1847A>G	XP_016883333.1:p.Lys616Arg
XM_017027845.1:c.920A>G	XP_016883334.1:p.Lys307Arg
NM_004518.6:c.1820A>G	NP_004509.2:p.Lys607Arg
NM_172106.3:c.1850A>G	NP_742104.1:p.Lys617Arg
NM_172107.4:c.1904A>G MANE Select	NP_742105.1:p.Lys635Arg
NM_172108.5:c.1811A>G	NP_742106.1:p.Lys604Arg
NM_001382235.1:c.1958A>G	NP_001369164.1:p.Lys653Arg