Canonical Allele Identifier: CA409639585

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038718A>C (hg19) ; chr20:g.63407365A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407365A>C , CM000682.2:g.63407365A>C	GRCh38
NC_000020.10:g.62038718A>C , CM000682.1:g.62038718A>C	GRCh37
NC_000020.9:g.61509162A>C	NCBI36
NG_009004.1:g.70276T>G
NG_009004.2:g.70276T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1952T>G	ENSP00000516702.1:p.Met651Arg
ENST00000359125.7:c.1898T>G MANE Select	ENSP00000352035.2:p.Met633Arg
ENST00000637193.1:c.1295T>G	ENSP00000490734.1:p.Met432Arg
ENST00000637338.1:n.55T>G
ENST00000344462.8:c.1805T>G	ENSP00000339611.4:p.Met602Arg
ENST00000357249.6:c.1466T>G	ENSP00000349789.3:p.Met489Arg
ENST00000359125.6:c.1898T>G	ENSP00000352035.2:p.Met633Arg
ENST00000360480.7:c.1814T>G	ENSP00000353668.3:p.Met605Arg
ENST00000370224.5:c.1922T>G	ENSP00000359244.2:p.Met641Arg
ENST00000625514.2:c.1886T>G	ENSP00000486040.1:p.Met629Arg
ENST00000626839.2:c.1844T>G	ENSP00000486706.1:p.Met615Arg
ENST00000629241.2:c.1814T>G	ENSP00000487142.1:p.Met605Arg
ENST00000629676.2:c.1679+6085T>G	ENSP00000486194.1:n.1679+6085T>G
NM_004518.4:c.1814T>G	NP_004509.2:p.Met605Arg
NM_172106.1:c.1844T>G	NP_742104.1:p.Met615Arg
NM_172107.2:c.1898T>G	NP_742105.1:p.Met633Arg
NM_172108.3:c.1805T>G	NP_742106.1:p.Met602Arg
XM_006723787.1:c.1940T>G	XP_006723850.1:p.Met647Arg
XM_011528807.1:c.2006T>G	XP_011527109.1:p.Met669Arg
XM_011528808.1:c.2003T>G	XP_011527110.1:p.Met668Arg
XM_011528809.1:c.1976T>G	XP_011527111.1:p.Met659Arg
XM_011528810.1:c.1952T>G	XP_011527112.1:p.Met651Arg
XM_011528811.1:c.1922T>G	XP_011527113.1:p.Met641Arg
XM_011528812.1:c.1895T>G	XP_011527114.1:p.Met632Arg
XM_011528813.1:c.1880T>G	XP_011527115.1:p.Met627Arg
XM_011528814.1:c.1487T>G	XP_011527116.1:p.Met496Arg
NM_004518.5:c.1814T>G	NP_004509.2:p.Met605Arg
NM_172106.2:c.1844T>G	NP_742104.1:p.Met615Arg
NM_172107.3:c.1898T>G	NP_742105.1:p.Met633Arg
NM_172108.4:c.1805T>G	NP_742106.1:p.Met602Arg
XM_011528810.2:c.1952T>G	XP_011527112.1:p.Met651Arg
XM_011528811.2:c.1922T>G	XP_011527113.1:p.Met641Arg
XM_017027841.2:c.1949T>G	XP_016883330.1:p.Met650Arg
XM_017027842.2:c.1886T>G	XP_016883331.1:p.Met629Arg
XM_017027843.1:c.1883T>G	XP_016883332.1:p.Met628Arg
XM_017027844.2:c.1841T>G	XP_016883333.1:p.Met614Arg
XM_017027845.1:c.914T>G	XP_016883334.1:p.Met305Arg
NM_004518.6:c.1814T>G	NP_004509.2:p.Met605Arg
NM_172106.3:c.1844T>G	NP_742104.1:p.Met615Arg
NM_172107.4:c.1898T>G MANE Select	NP_742105.1:p.Met633Arg
NM_172108.5:c.1805T>G	NP_742106.1:p.Met602Arg
NM_001382235.1:c.1952T>G	NP_001369164.1:p.Met651Arg