Canonical Allele Identifier: CA511339651

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038696C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407343C>A , CM000682.2:g.63407343C>A	GRCh38
NC_000020.10:g.62038696C>A , CM000682.1:g.62038696C>A	GRCh37
NC_000020.9:g.61509140C>A	NCBI36
NG_009004.1:g.70298G>T
NG_009004.2:g.70298G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1974G>T	ENSP00000516702.1:p.Leu658=
ENST00000359125.7:c.1920G>T MANE Select	ENSP00000352035.2:p.Leu640=
ENST00000637193.1:c.1317G>T	ENSP00000490734.1:p.Leu439=
ENST00000637338.1:n.77G>T
ENST00000344462.8:c.1827G>T	ENSP00000339611.4:p.Leu609=
ENST00000357249.6:c.1488G>T	ENSP00000349789.3:p.Leu496=
ENST00000359125.6:c.1920G>T	ENSP00000352035.2:p.Leu640=
ENST00000360480.7:c.1836G>T	ENSP00000353668.3:p.Leu612=
ENST00000370224.5:c.1944G>T	ENSP00000359244.2:p.Leu648=
ENST00000625514.2:c.1908G>T	ENSP00000486040.1:p.Leu636=
ENST00000626839.2:c.1866G>T	ENSP00000486706.1:p.Leu622=
ENST00000629241.2:c.1836G>T	ENSP00000487142.1:p.Leu612=
ENST00000629676.2:c.1679+6107G>T	ENSP00000486194.1:n.1679+6107G>T
NM_004518.4:c.1836G>T	NP_004509.2:p.Leu612=
NM_172106.1:c.1866G>T	NP_742104.1:p.Leu622=
NM_172107.2:c.1920G>T	NP_742105.1:p.Leu640=
NM_172108.3:c.1827G>T	NP_742106.1:p.Leu609=
XM_006723787.1:c.1962G>T	XP_006723850.1:p.Leu654=
XM_011528807.1:c.2028G>T	XP_011527109.1:p.Leu676=
XM_011528808.1:c.2025G>T	XP_011527110.1:p.Leu675=
XM_011528809.1:c.1998G>T	XP_011527111.1:p.Leu666=
XM_011528810.1:c.1974G>T	XP_011527112.1:p.Leu658=
XM_011528811.1:c.1944G>T	XP_011527113.1:p.Leu648=
XM_011528812.1:c.1917G>T	XP_011527114.1:p.Leu639=
XM_011528813.1:c.1902G>T	XP_011527115.1:p.Leu634=
XM_011528814.1:c.1509G>T	XP_011527116.1:p.Leu503=
NM_004518.5:c.1836G>T	NP_004509.2:p.Leu612=
NM_172106.2:c.1866G>T	NP_742104.1:p.Leu622=
NM_172107.3:c.1920G>T	NP_742105.1:p.Leu640=
NM_172108.4:c.1827G>T	NP_742106.1:p.Leu609=
XM_011528810.2:c.1974G>T	XP_011527112.1:p.Leu658=
XM_011528811.2:c.1944G>T	XP_011527113.1:p.Leu648=
XM_017027841.2:c.1971G>T	XP_016883330.1:p.Leu657=
XM_017027842.2:c.1908G>T	XP_016883331.1:p.Leu636=
XM_017027843.1:c.1905G>T	XP_016883332.1:p.Leu635=
XM_017027844.2:c.1863G>T	XP_016883333.1:p.Leu621=
XM_017027845.1:c.936G>T	XP_016883334.1:p.Leu312=
NM_004518.6:c.1836G>T	NP_004509.2:p.Leu612=
NM_172106.3:c.1866G>T	NP_742104.1:p.Leu622=
NM_172107.4:c.1920G>T MANE Select	NP_742105.1:p.Leu640=
NM_172108.5:c.1827G>T	NP_742106.1:p.Leu609=
NM_001382235.1:c.1974G>T	NP_001369164.1:p.Leu658=