Canonical Allele Identifier: CA409638498

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038407C>G (hg19) ; chr20:g.63407054C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407054C>G , CM000682.2:g.63407054C>G	GRCh38
NC_000020.10:g.62038407C>G , CM000682.1:g.62038407C>G	GRCh37
NC_000020.9:g.61508851C>G	NCBI36
NG_009004.1:g.70587G>C
NG_009004.2:g.70587G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2263G>C	ENSP00000516702.1:p.Gly755Arg
ENST00000359125.7:c.2209G>C MANE Select	ENSP00000352035.2:p.Gly737Arg
ENST00000637193.1:c.1606G>C	ENSP00000490734.1:p.Gly536Arg
ENST00000344462.8:c.2116G>C	ENSP00000339611.4:p.Gly706Arg
ENST00000357249.6:c.1777G>C	ENSP00000349789.3:p.Gly593Arg
ENST00000359125.6:c.2209G>C	ENSP00000352035.2:p.Gly737Arg
ENST00000360480.7:c.2125G>C	ENSP00000353668.3:p.Gly709Arg
ENST00000370224.5:c.2233G>C	ENSP00000359244.2:p.Gly745Arg
ENST00000625514.2:c.2197G>C	ENSP00000486040.1:p.Gly733Arg
ENST00000626839.2:c.2155G>C	ENSP00000486706.1:p.Gly719Arg
ENST00000629241.2:c.2125G>C	ENSP00000487142.1:p.Gly709Arg
ENST00000629676.2:c.1680-6211G>C	ENSP00000486194.1:n.1680-6211G>C
NM_004518.4:c.2125G>C	NP_004509.2:p.Gly709Arg
NM_172106.1:c.2155G>C	NP_742104.1:p.Gly719Arg
NM_172107.2:c.2209G>C	NP_742105.1:p.Gly737Arg
NM_172108.3:c.2116G>C	NP_742106.1:p.Gly706Arg
XM_006723787.1:c.2251G>C	XP_006723850.1:p.Gly751Arg
XM_011528807.1:c.2317G>C	XP_011527109.1:p.Gly773Arg
XM_011528808.1:c.2314G>C	XP_011527110.1:p.Gly772Arg
XM_011528809.1:c.2287G>C	XP_011527111.1:p.Gly763Arg
XM_011528810.1:c.2263G>C	XP_011527112.1:p.Gly755Arg
XM_011528811.1:c.2233G>C	XP_011527113.1:p.Gly745Arg
XM_011528812.1:c.2206G>C	XP_011527114.1:p.Gly736Arg
XM_011528813.1:c.2191G>C	XP_011527115.1:p.Gly731Arg
XM_011528814.1:c.1798G>C	XP_011527116.1:p.Gly600Arg
NM_004518.5:c.2125G>C	NP_004509.2:p.Gly709Arg
NM_172106.2:c.2155G>C	NP_742104.1:p.Gly719Arg
NM_172107.3:c.2209G>C	NP_742105.1:p.Gly737Arg
NM_172108.4:c.2116G>C	NP_742106.1:p.Gly706Arg
XM_011528810.2:c.2263G>C	XP_011527112.1:p.Gly755Arg
XM_011528811.2:c.2233G>C	XP_011527113.1:p.Gly745Arg
XM_017027841.2:c.2260G>C	XP_016883330.1:p.Gly754Arg
XM_017027842.2:c.2197G>C	XP_016883331.1:p.Gly733Arg
XM_017027843.1:c.2194G>C	XP_016883332.1:p.Gly732Arg
XM_017027844.2:c.2152G>C	XP_016883333.1:p.Gly718Arg
XM_017027845.1:c.1225G>C	XP_016883334.1:p.Gly409Arg
NM_004518.6:c.2125G>C	NP_004509.2:p.Gly709Arg
NM_172106.3:c.2155G>C	NP_742104.1:p.Gly719Arg
NM_172107.4:c.2209G>C MANE Select	NP_742105.1:p.Gly737Arg
NM_172108.5:c.2116G>C	NP_742106.1:p.Gly706Arg
NM_001382235.1:c.2263G>C	NP_001369164.1:p.Gly755Arg