Canonical Allele Identifier: CA2374777986

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63413555C= , CM000682.2:g.63413555C=	GRCh38
NC_000020.10:g.62044908C= , CM000682.1:g.62044908C=	GRCh37
NC_000020.9:g.61515352C=	NCBI36
NG_009004.1:g.64086G=
NG_009004.2:g.64086G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1604G=	ENSP00000516702.1:p.Arg535=
ENST00000359125.7:c.1658G= MANE Select	ENSP00000352035.2:p.Arg553=
ENST00000637193.1:c.1055G=	ENSP00000490734.1:p.Arg352=
ENST00000344462.8:c.1565G=	ENSP00000339611.4:p.Arg522=
ENST00000357249.6:c.1226G=	ENSP00000349789.3:p.Arg409=
ENST00000359125.6:c.1658G=	ENSP00000352035.2:p.Arg553=
ENST00000360480.7:c.1574G=	ENSP00000353668.3:p.Arg525=
ENST00000370224.5:c.1574G=	ENSP00000359244.2:p.Arg525=
ENST00000625514.2:c.1538G=	ENSP00000486040.1:p.Arg513=
ENST00000626839.2:c.1604G=	ENSP00000486706.1:p.Arg535=
ENST00000629241.2:c.1574G=	ENSP00000487142.1:p.Arg525=
ENST00000629318.1:c.266G=	ENSP00000487384.1:p.Arg89=
ENST00000629676.2:c.1574G=	ENSP00000486194.1:p.Arg525=
NM_004518.4:c.1574G=	NP_004509.2:p.Arg525=
NM_172106.1:c.1604G=	NP_742104.1:p.Arg535=
NM_172107.2:c.1658G=	NP_742105.1:p.Arg553=
NM_172108.3:c.1565G=	NP_742106.1:p.Arg522=
XM_006723787.1:c.1658G=	XP_006723850.1:p.Arg553=
XM_011528807.1:c.1658G=	XP_011527109.1:p.Arg553=
XM_011528808.1:c.1655G=	XP_011527110.1:p.Arg552=
XM_011528809.1:c.1628G=	XP_011527111.1:p.Arg543=
XM_011528810.1:c.1604G=	XP_011527112.1:p.Arg535=
XM_011528811.1:c.1574G=	XP_011527113.1:p.Arg525=
XM_011528812.1:c.1655G=	XP_011527114.1:p.Arg552=
XM_011528813.1:c.1532G=	XP_011527115.1:p.Arg511=
XM_011528814.1:c.1139G=	XP_011527116.1:p.Arg380=
XM_011528815.1:c.1658G=	XP_011527117.1:p.Arg553=
NM_004518.5:c.1574G=	NP_004509.2:p.Arg525=
NM_172106.2:c.1604G=	NP_742104.1:p.Arg535=
NM_172107.3:c.1658G=	NP_742105.1:p.Arg553=
NM_172108.4:c.1565G=	NP_742106.1:p.Arg522=
XM_011528810.2:c.1604G=	XP_011527112.1:p.Arg535=
XM_011528811.2:c.1574G=	XP_011527113.1:p.Arg525=
XM_017027841.2:c.1601G=	XP_016883330.1:p.Arg534=
XM_017027842.2:c.1604G=	XP_016883331.1:p.Arg535=
XM_017027843.1:c.1535G=	XP_016883332.1:p.Arg512=
XM_017027844.2:c.1601G=	XP_016883333.1:p.Arg534=
XM_017027845.1:c.566G=	XP_016883334.1:p.Arg189=
NM_004518.6:c.1574G=	NP_004509.2:p.Arg525=
NM_172106.3:c.1604G=	NP_742104.1:p.Arg535=
NM_172107.4:c.1658G= MANE Select	NP_742105.1:p.Arg553=
NM_172108.5:c.1565G=	NP_742106.1:p.Arg522=
NM_001382235.1:c.1604G=	NP_001369164.1:p.Arg535=