Canonical Allele Identifier: CA409637978

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038325T>G (hg19) ; chr20:g.63406972T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406972T>G , CM000682.2:g.63406972T>G	GRCh38
NC_000020.10:g.62038325T>G , CM000682.1:g.62038325T>G	GRCh37
NC_000020.9:g.61508769T>G	NCBI36
NG_009004.1:g.70669A>C
NG_009004.2:g.70669A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2345A>C	ENSP00000516702.1:p.Glu782Ala
ENST00000359125.7:c.2291A>C MANE Select	ENSP00000352035.2:p.Glu764Ala
ENST00000637193.1:c.1688A>C	ENSP00000490734.1:p.Glu563Ala
ENST00000344462.8:c.2198A>C	ENSP00000339611.4:p.Glu733Ala
ENST00000357249.6:c.1859A>C	ENSP00000349789.3:p.Glu620Ala
ENST00000359125.6:c.2291A>C	ENSP00000352035.2:p.Glu764Ala
ENST00000360480.7:c.2207A>C	ENSP00000353668.3:p.Glu736Ala
ENST00000370224.5:c.2241+74A>C	ENSP00000359244.2:n.2241+74A>C
ENST00000625514.2:c.2205+74A>C	ENSP00000486040.1:n.2205+74A>C
ENST00000626839.2:c.2237A>C	ENSP00000486706.1:p.Glu746Ala
ENST00000629241.2:c.2133+74A>C	ENSP00000487142.1:n.2133+74A>C
ENST00000629676.2:c.1680-6129A>C	ENSP00000486194.1:n.1680-6129A>C
NM_004518.4:c.2207A>C	NP_004509.2:p.Glu736Ala
NM_172106.1:c.2237A>C	NP_742104.1:p.Glu746Ala
NM_172107.2:c.2291A>C	NP_742105.1:p.Glu764Ala
NM_172108.3:c.2198A>C	NP_742106.1:p.Glu733Ala
XM_006723787.1:c.2333A>C	XP_006723850.1:p.Glu778Ala
XM_011528807.1:c.2399A>C	XP_011527109.1:p.Glu800Ala
XM_011528808.1:c.2396A>C	XP_011527110.1:p.Glu799Ala
XM_011528809.1:c.2369A>C	XP_011527111.1:p.Glu790Ala
XM_011528810.1:c.2345A>C	XP_011527112.1:p.Glu782Ala
XM_011528811.1:c.2315A>C	XP_011527113.1:p.Glu772Ala
XM_011528812.1:c.2288A>C	XP_011527114.1:p.Glu763Ala
XM_011528813.1:c.2273A>C	XP_011527115.1:p.Glu758Ala
XM_011528814.1:c.1880A>C	XP_011527116.1:p.Glu627Ala
NM_004518.5:c.2207A>C	NP_004509.2:p.Glu736Ala
NM_172106.2:c.2237A>C	NP_742104.1:p.Glu746Ala
NM_172107.3:c.2291A>C	NP_742105.1:p.Glu764Ala
NM_172108.4:c.2198A>C	NP_742106.1:p.Glu733Ala
XM_011528810.2:c.2345A>C	XP_011527112.1:p.Glu782Ala
XM_011528811.2:c.2315A>C	XP_011527113.1:p.Glu772Ala
XM_017027841.2:c.2342A>C	XP_016883330.1:p.Glu781Ala
XM_017027842.2:c.2279A>C	XP_016883331.1:p.Glu760Ala
XM_017027843.1:c.2276A>C	XP_016883332.1:p.Glu759Ala
XM_017027844.2:c.2234A>C	XP_016883333.1:p.Glu745Ala
XM_017027845.1:c.1307A>C	XP_016883334.1:p.Glu436Ala
NM_004518.6:c.2207A>C	NP_004509.2:p.Glu736Ala
NM_172106.3:c.2237A>C	NP_742104.1:p.Glu746Ala
NM_172107.4:c.2291A>C MANE Select	NP_742105.1:p.Glu764Ala
NM_172108.5:c.2198A>C	NP_742106.1:p.Glu733Ala
NM_001382235.1:c.2345A>C	NP_001369164.1:p.Glu782Ala