Canonical Allele Identifier: CA409645530

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62045503G>T (hg19) ; chr20:g.63414150G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414150G>T , CM000682.2:g.63414150G>T	GRCh38
NC_000020.10:g.62045503G>T , CM000682.1:g.62045503G>T	GRCh37
NC_000020.9:g.61515947G>T	NCBI36
NG_009004.1:g.63491C>A
NG_009004.2:g.63491C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1515C>A	ENSP00000516702.1:p.Cys505Ter
ENST00000359125.7:c.1569C>A MANE Select	ENSP00000352035.2:p.Cys523Ter
ENST00000637193.1:c.966C>A	ENSP00000490734.1:p.Cys322Ter
ENST00000344462.8:c.1476C>A	ENSP00000339611.4:p.Cys492Ter
ENST00000357249.6:c.1137C>A	ENSP00000349789.3:p.Cys379Ter
ENST00000359125.6:c.1569C>A	ENSP00000352035.2:p.Cys523Ter
ENST00000360480.7:c.1485C>A	ENSP00000353668.3:p.Cys495Ter
ENST00000370224.5:c.1485C>A	ENSP00000359244.2:p.Cys495Ter
ENST00000625514.2:c.1449C>A	ENSP00000486040.1:p.Cys483Ter
ENST00000626839.2:c.1515C>A	ENSP00000486706.1:p.Cys505Ter
ENST00000627221.2:c.626C>A
ENST00000629241.2:c.1485C>A	ENSP00000487142.1:p.Cys495Ter
ENST00000629318.1:c.177C>A	ENSP00000487384.1:p.Cys59Ter
ENST00000629676.2:c.1485C>A	ENSP00000486194.1:p.Cys495Ter
NM_004518.4:c.1485C>A	NP_004509.2:p.Cys495Ter
NM_172106.1:c.1515C>A	NP_742104.1:p.Cys505Ter
NM_172107.2:c.1569C>A	NP_742105.1:p.Cys523Ter
NM_172108.3:c.1476C>A	NP_742106.1:p.Cys492Ter
XM_006723787.1:c.1569C>A	XP_006723850.1:p.Cys523Ter
XM_011528807.1:c.1569C>A	XP_011527109.1:p.Cys523Ter
XM_011528808.1:c.1566C>A	XP_011527110.1:p.Cys522Ter
XM_011528809.1:c.1539C>A	XP_011527111.1:p.Cys513Ter
XM_011528810.1:c.1515C>A	XP_011527112.1:p.Cys505Ter
XM_011528811.1:c.1485C>A	XP_011527113.1:p.Cys495Ter
XM_011528812.1:c.1566C>A	XP_011527114.1:p.Cys522Ter
XM_011528813.1:c.1443C>A	XP_011527115.1:p.Cys481Ter
XM_011528814.1:c.1050C>A	XP_011527116.1:p.Cys350Ter
XM_011528815.1:c.1569C>A	XP_011527117.1:p.Cys523Ter
NM_004518.5:c.1485C>A	NP_004509.2:p.Cys495Ter
NM_172106.2:c.1515C>A	NP_742104.1:p.Cys505Ter
NM_172107.3:c.1569C>A	NP_742105.1:p.Cys523Ter
NM_172108.4:c.1476C>A	NP_742106.1:p.Cys492Ter
XM_011528810.2:c.1515C>A	XP_011527112.1:p.Cys505Ter
XM_011528811.2:c.1485C>A	XP_011527113.1:p.Cys495Ter
XM_017027841.2:c.1512C>A	XP_016883330.1:p.Cys504Ter
XM_017027842.2:c.1515C>A	XP_016883331.1:p.Cys505Ter
XM_017027843.1:c.1446C>A	XP_016883332.1:p.Cys482Ter
XM_017027844.2:c.1512C>A	XP_016883333.1:p.Cys504Ter
XM_017027845.1:c.477C>A	XP_016883334.1:p.Cys159Ter
NM_004518.6:c.1485C>A	NP_004509.2:p.Cys495Ter
NM_172106.3:c.1515C>A	NP_742104.1:p.Cys505Ter
NM_172107.4:c.1569C>A MANE Select	NP_742105.1:p.Cys523Ter
NM_172108.5:c.1476C>A	NP_742106.1:p.Cys492Ter
NM_001382235.1:c.1515C>A	NP_001369164.1:p.Cys505Ter