Canonical Allele Identifier: CA409639149

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63407235-G-C
• MyVariant Identifiers: chr20:g.62038588G>C (hg19) ; chr20:g.63407235G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407235G>C , CM000682.2:g.63407235G>C	GRCh38
NC_000020.10:g.62038588G>C , CM000682.1:g.62038588G>C	GRCh37
NC_000020.9:g.61509032G>C	NCBI36
NG_009004.1:g.70406C>G
NG_009004.2:g.70406C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000706989.1:c.2082C>G	ENSP00000516702.1:p.Ser694Arg
ENST00000359125.7:c.2028C>G MANE Select	ENSP00000352035.2:p.Ser676Arg
ENST00000637193.1:c.1425C>G	ENSP00000490734.1:p.Ser475Arg
ENST00000344462.8:c.1935C>G	ENSP00000339611.4:p.Ser645Arg
ENST00000357249.6:c.1596C>G	ENSP00000349789.3:p.Ser532Arg
ENST00000359125.6:c.2028C>G	ENSP00000352035.2:p.Ser676Arg
ENST00000360480.7:c.1944C>G	ENSP00000353668.3:p.Ser648Arg
ENST00000370224.5:c.2052C>G	ENSP00000359244.2:p.Ser684Arg
ENST00000625514.2:c.2016C>G	ENSP00000486040.1:p.Ser672Arg
ENST00000626839.2:c.1974C>G	ENSP00000486706.1:p.Ser658Arg
ENST00000629241.2:c.1944C>G	ENSP00000487142.1:p.Ser648Arg
ENST00000629676.2:c.1679+6215C>G	ENSP00000486194.1:n.1679+6215C>G
NM_004518.4:c.1944C>G	NP_004509.2:p.Ser648Arg
NM_172106.1:c.1974C>G	NP_742104.1:p.Ser658Arg
NM_172107.2:c.2028C>G	NP_742105.1:p.Ser676Arg
NM_172108.3:c.1935C>G	NP_742106.1:p.Ser645Arg
XM_006723787.1:c.2070C>G	XP_006723850.1:p.Ser690Arg
XM_011528807.1:c.2136C>G	XP_011527109.1:p.Ser712Arg
XM_011528808.1:c.2133C>G	XP_011527110.1:p.Ser711Arg
XM_011528809.1:c.2106C>G	XP_011527111.1:p.Ser702Arg
XM_011528810.1:c.2082C>G	XP_011527112.1:p.Ser694Arg
XM_011528811.1:c.2052C>G	XP_011527113.1:p.Ser684Arg
XM_011528812.1:c.2025C>G	XP_011527114.1:p.Ser675Arg
XM_011528813.1:c.2010C>G	XP_011527115.1:p.Ser670Arg
XM_011528814.1:c.1617C>G	XP_011527116.1:p.Ser539Arg
NM_004518.5:c.1944C>G	NP_004509.2:p.Ser648Arg
NM_172106.2:c.1974C>G	NP_742104.1:p.Ser658Arg
NM_172107.3:c.2028C>G	NP_742105.1:p.Ser676Arg
NM_172108.4:c.1935C>G	NP_742106.1:p.Ser645Arg
XM_011528810.2:c.2082C>G	XP_011527112.1:p.Ser694Arg
XM_011528811.2:c.2052C>G	XP_011527113.1:p.Ser684Arg
XM_017027841.2:c.2079C>G	XP_016883330.1:p.Ser693Arg
XM_017027842.2:c.2016C>G	XP_016883331.1:p.Ser672Arg
XM_017027843.1:c.2013C>G	XP_016883332.1:p.Ser671Arg
XM_017027844.2:c.1971C>G	XP_016883333.1:p.Ser657Arg
XM_017027845.1:c.1044C>G	XP_016883334.1:p.Ser348Arg
NM_004518.6:c.1944C>G	NP_004509.2:p.Ser648Arg
NM_172106.3:c.1974C>G	NP_742104.1:p.Ser658Arg
NM_172107.4:c.2028C>G MANE Select	NP_742105.1:p.Ser676Arg
NM_172108.5:c.1935C>G	NP_742106.1:p.Ser645Arg
NM_001382235.1:c.2082C>G	NP_001369164.1:p.Ser694Arg