Canonical Allele Identifier: CA2374778289

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414100A= , CM000682.2:g.63414100A=	GRCh38
NC_000020.10:g.62045453A= , CM000682.1:g.62045453A=	GRCh37
NC_000020.9:g.61515897A=	NCBI36
NG_009004.1:g.63541T=
NG_009004.2:g.63541T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1565T=	ENSP00000516702.1:p.Ile522=
ENST00000359125.7:c.1619T= MANE Select	ENSP00000352035.2:p.Ile540=
ENST00000637193.1:c.1016T=	ENSP00000490734.1:p.Ile339=
ENST00000344462.8:c.1526T=	ENSP00000339611.4:p.Ile509=
ENST00000357249.6:c.1187T=	ENSP00000349789.3:p.Ile396=
ENST00000359125.6:c.1619T=	ENSP00000352035.2:p.Ile540=
ENST00000360480.7:c.1535T=	ENSP00000353668.3:p.Ile512=
ENST00000370224.5:c.1535T=	ENSP00000359244.2:p.Ile512=
ENST00000625514.2:c.1499T=	ENSP00000486040.1:p.Ile500=
ENST00000626839.2:c.1565T=	ENSP00000486706.1:p.Ile522=
ENST00000627221.2:c.676T=
ENST00000629241.2:c.1535T=	ENSP00000487142.1:p.Ile512=
ENST00000629318.1:c.227T=	ENSP00000487384.1:p.Ile76=
ENST00000629676.2:c.1535T=	ENSP00000486194.1:p.Ile512=
NM_004518.4:c.1535T=	NP_004509.2:p.Ile512=
NM_172106.1:c.1565T=	NP_742104.1:p.Ile522=
NM_172107.2:c.1619T=	NP_742105.1:p.Ile540=
NM_172108.3:c.1526T=	NP_742106.1:p.Ile509=
XM_006723787.1:c.1619T=	XP_006723850.1:p.Ile540=
XM_011528807.1:c.1619T=	XP_011527109.1:p.Ile540=
XM_011528808.1:c.1616T=	XP_011527110.1:p.Ile539=
XM_011528809.1:c.1589T=	XP_011527111.1:p.Ile530=
XM_011528810.1:c.1565T=	XP_011527112.1:p.Ile522=
XM_011528811.1:c.1535T=	XP_011527113.1:p.Ile512=
XM_011528812.1:c.1616T=	XP_011527114.1:p.Ile539=
XM_011528813.1:c.1493T=	XP_011527115.1:p.Ile498=
XM_011528814.1:c.1100T=	XP_011527116.1:p.Ile367=
XM_011528815.1:c.1619T=	XP_011527117.1:p.Ile540=
NM_004518.5:c.1535T=	NP_004509.2:p.Ile512=
NM_172106.2:c.1565T=	NP_742104.1:p.Ile522=
NM_172107.3:c.1619T=	NP_742105.1:p.Ile540=
NM_172108.4:c.1526T=	NP_742106.1:p.Ile509=
XM_011528810.2:c.1565T=	XP_011527112.1:p.Ile522=
XM_011528811.2:c.1535T=	XP_011527113.1:p.Ile512=
XM_017027841.2:c.1562T=	XP_016883330.1:p.Ile521=
XM_017027842.2:c.1565T=	XP_016883331.1:p.Ile522=
XM_017027843.1:c.1496T=	XP_016883332.1:p.Ile499=
XM_017027844.2:c.1562T=	XP_016883333.1:p.Ile521=
XM_017027845.1:c.527T=	XP_016883334.1:p.Ile176=
NM_004518.6:c.1535T=	NP_004509.2:p.Ile512=
NM_172106.3:c.1565T=	NP_742104.1:p.Ile522=
NM_172107.4:c.1619T= MANE Select	NP_742105.1:p.Ile540=
NM_172108.5:c.1526T=	NP_742106.1:p.Ile509=
NM_001382235.1:c.1565T=	NP_001369164.1:p.Ile522=