Canonical Allele Identifier: CA409639048

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63407188-G-T
• MyVariant Identifiers: chr20:g.62038541G>T (hg19) ; chr20:g.63407188G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407188G>T , CM000682.2:g.63407188G>T	GRCh38
NC_000020.10:g.62038541G>T , CM000682.1:g.62038541G>T	GRCh37
NC_000020.9:g.61508985G>T	NCBI36
NG_009004.1:g.70453C>A
NG_009004.2:g.70453C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2129C>A	ENSP00000516702.1:p.Ser710Tyr
ENST00000359125.7:c.2075C>A MANE Select	ENSP00000352035.2:p.Ser692Tyr
ENST00000637193.1:c.1472C>A	ENSP00000490734.1:p.Ser491Tyr
ENST00000344462.8:c.1982C>A	ENSP00000339611.4:p.Ser661Tyr
ENST00000357249.6:c.1643C>A	ENSP00000349789.3:p.Ser548Tyr
ENST00000359125.6:c.2075C>A	ENSP00000352035.2:p.Ser692Tyr
ENST00000360480.7:c.1991C>A	ENSP00000353668.3:p.Ser664Tyr
ENST00000370224.5:c.2099C>A	ENSP00000359244.2:p.Ser700Tyr
ENST00000625514.2:c.2063C>A	ENSP00000486040.1:p.Ser688Tyr
ENST00000626839.2:c.2021C>A	ENSP00000486706.1:p.Ser674Tyr
ENST00000629241.2:c.1991C>A	ENSP00000487142.1:p.Ser664Tyr
ENST00000629676.2:c.1679+6262C>A	ENSP00000486194.1:n.1679+6262C>A
NM_004518.4:c.1991C>A	NP_004509.2:p.Ser664Tyr
NM_172106.1:c.2021C>A	NP_742104.1:p.Ser674Tyr
NM_172107.2:c.2075C>A	NP_742105.1:p.Ser692Tyr
NM_172108.3:c.1982C>A	NP_742106.1:p.Ser661Tyr
XM_006723787.1:c.2117C>A	XP_006723850.1:p.Ser706Tyr
XM_011528807.1:c.2183C>A	XP_011527109.1:p.Ser728Tyr
XM_011528808.1:c.2180C>A	XP_011527110.1:p.Ser727Tyr
XM_011528809.1:c.2153C>A	XP_011527111.1:p.Ser718Tyr
XM_011528810.1:c.2129C>A	XP_011527112.1:p.Ser710Tyr
XM_011528811.1:c.2099C>A	XP_011527113.1:p.Ser700Tyr
XM_011528812.1:c.2072C>A	XP_011527114.1:p.Ser691Tyr
XM_011528813.1:c.2057C>A	XP_011527115.1:p.Ser686Tyr
XM_011528814.1:c.1664C>A	XP_011527116.1:p.Ser555Tyr
NM_004518.5:c.1991C>A	NP_004509.2:p.Ser664Tyr
NM_172106.2:c.2021C>A	NP_742104.1:p.Ser674Tyr
NM_172107.3:c.2075C>A	NP_742105.1:p.Ser692Tyr
NM_172108.4:c.1982C>A	NP_742106.1:p.Ser661Tyr
XM_011528810.2:c.2129C>A	XP_011527112.1:p.Ser710Tyr
XM_011528811.2:c.2099C>A	XP_011527113.1:p.Ser700Tyr
XM_017027841.2:c.2126C>A	XP_016883330.1:p.Ser709Tyr
XM_017027842.2:c.2063C>A	XP_016883331.1:p.Ser688Tyr
XM_017027843.1:c.2060C>A	XP_016883332.1:p.Ser687Tyr
XM_017027844.2:c.2018C>A	XP_016883333.1:p.Ser673Tyr
XM_017027845.1:c.1091C>A	XP_016883334.1:p.Ser364Tyr
NM_004518.6:c.1991C>A	NP_004509.2:p.Ser664Tyr
NM_172106.3:c.2021C>A	NP_742104.1:p.Ser674Tyr
NM_172107.4:c.2075C>A MANE Select	NP_742105.1:p.Ser692Tyr
NM_172108.5:c.1982C>A	NP_742106.1:p.Ser661Tyr
NM_001382235.1:c.2129C>A	NP_001369164.1:p.Ser710Tyr