Canonical Allele Identifier: CA2374778845

Gene: KCNQ2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63415080C= , CM000682.2:g.63415080C=	GRCh38
NC_000020.10:g.62046433C= , CM000682.1:g.62046433C=	GRCh37
NC_000020.9:g.61516877C=	NCBI36
NG_009004.1:g.62561G=
NG_009004.2:g.62561G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1294G=	ENSP00000516702.1:p.Val432=
ENST00000359125.7:c.1348G= MANE Select	ENSP00000352035.2:p.Val450=
ENST00000637193.1:c.745G=	ENSP00000490734.1:p.Val249=
ENST00000637584.1:n.85G=
ENST00000344462.8:c.1258G=	ENSP00000339611.4:p.Val420=
ENST00000357249.6:c.916G=	ENSP00000349789.3:p.Val306=
ENST00000359125.6:c.1348G=	ENSP00000352035.2:p.Val450=
ENST00000360480.7:c.1264G=	ENSP00000353668.3:p.Val422=
ENST00000370224.5:c.1264G=	ENSP00000359244.2:p.Val422=
ENST00000625514.2:c.1228G=	ENSP00000486040.1:p.Val410=
ENST00000626839.2:c.1294G=	ENSP00000486706.1:p.Val432=
ENST00000627221.2:c.408G=
ENST00000629241.2:c.1264G=	ENSP00000487142.1:p.Val422=
ENST00000629676.2:c.1264G=	ENSP00000486194.1:p.Val422=
NM_004518.4:c.1264G=	NP_004509.2:p.Val422=
NM_172106.1:c.1294G=	NP_742104.1:p.Val432=
NM_172107.2:c.1348G=	NP_742105.1:p.Val450=
NM_172108.3:c.1258G=	NP_742106.1:p.Val420=
XM_006723787.1:c.1348G=	XP_006723850.1:p.Val450=
XM_011528807.1:c.1348G=	XP_011527109.1:p.Val450=
XM_011528808.1:c.1348G=	XP_011527110.1:p.Val450=
XM_011528809.1:c.1318G=	XP_011527111.1:p.Val440=
XM_011528810.1:c.1294G=	XP_011527112.1:p.Val432=
XM_011528811.1:c.1264G=	XP_011527113.1:p.Val422=
XM_011528812.1:c.1348G=	XP_011527114.1:p.Val450=
XM_011528813.1:c.1222G=	XP_011527115.1:p.Val408=
XM_011528814.1:c.829G=	XP_011527116.1:p.Val277=
XM_011528815.1:c.1348G=	XP_011527117.1:p.Val450=
NM_004518.5:c.1264G=	NP_004509.2:p.Val422=
NM_172106.2:c.1294G=	NP_742104.1:p.Val432=
NM_172107.3:c.1348G=	NP_742105.1:p.Val450=
NM_172108.4:c.1258G=	NP_742106.1:p.Val420=
XM_011528810.2:c.1294G=	XP_011527112.1:p.Val432=
XM_011528811.2:c.1264G=	XP_011527113.1:p.Val422=
XM_017027841.2:c.1294G=	XP_016883330.1:p.Val432=
XM_017027842.2:c.1294G=	XP_016883331.1:p.Val432=
XM_017027843.1:c.1225G=	XP_016883332.1:p.Val409=
XM_017027844.2:c.1294G=	XP_016883333.1:p.Val432=
XM_017027845.1:c.256G=	XP_016883334.1:p.Val86=
NM_004518.6:c.1264G=	NP_004509.2:p.Val422=
NM_172106.3:c.1294G=	NP_742104.1:p.Val432=
NM_172107.4:c.1348G= MANE Select	NP_742105.1:p.Val450=
NM_172108.5:c.1258G=	NP_742106.1:p.Val420=
NM_001382235.1:c.1294G=	NP_001369164.1:p.Val432=