Canonical Allele Identifier: CA409645533

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62045504C>A (hg19) ; chr20:g.63414151C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414151C>A , CM000682.2:g.63414151C>A	GRCh38
NC_000020.10:g.62045504C>A , CM000682.1:g.62045504C>A	GRCh37
NC_000020.9:g.61515948C>A	NCBI36
NG_009004.1:g.63490G>T
NG_009004.2:g.63490G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1514G>T	ENSP00000516702.1:p.Cys505Phe
ENST00000359125.7:c.1568G>T MANE Select	ENSP00000352035.2:p.Cys523Phe
ENST00000637193.1:c.965G>T	ENSP00000490734.1:p.Cys322Phe
ENST00000344462.8:c.1475G>T	ENSP00000339611.4:p.Cys492Phe
ENST00000357249.6:c.1136G>T	ENSP00000349789.3:p.Cys379Phe
ENST00000359125.6:c.1568G>T	ENSP00000352035.2:p.Cys523Phe
ENST00000360480.7:c.1484G>T	ENSP00000353668.3:p.Cys495Phe
ENST00000370224.5:c.1484G>T	ENSP00000359244.2:p.Cys495Phe
ENST00000625514.2:c.1448G>T	ENSP00000486040.1:p.Cys483Phe
ENST00000626839.2:c.1514G>T	ENSP00000486706.1:p.Cys505Phe
ENST00000627221.2:c.625G>T
ENST00000629241.2:c.1484G>T	ENSP00000487142.1:p.Cys495Phe
ENST00000629318.1:c.176G>T	ENSP00000487384.1:p.Cys59Phe
ENST00000629676.2:c.1484G>T	ENSP00000486194.1:p.Cys495Phe
NM_004518.4:c.1484G>T	NP_004509.2:p.Cys495Phe
NM_172106.1:c.1514G>T	NP_742104.1:p.Cys505Phe
NM_172107.2:c.1568G>T	NP_742105.1:p.Cys523Phe
NM_172108.3:c.1475G>T	NP_742106.1:p.Cys492Phe
XM_006723787.1:c.1568G>T	XP_006723850.1:p.Cys523Phe
XM_011528807.1:c.1568G>T	XP_011527109.1:p.Cys523Phe
XM_011528808.1:c.1565G>T	XP_011527110.1:p.Cys522Phe
XM_011528809.1:c.1538G>T	XP_011527111.1:p.Cys513Phe
XM_011528810.1:c.1514G>T	XP_011527112.1:p.Cys505Phe
XM_011528811.1:c.1484G>T	XP_011527113.1:p.Cys495Phe
XM_011528812.1:c.1565G>T	XP_011527114.1:p.Cys522Phe
XM_011528813.1:c.1442G>T	XP_011527115.1:p.Cys481Phe
XM_011528814.1:c.1049G>T	XP_011527116.1:p.Cys350Phe
XM_011528815.1:c.1568G>T	XP_011527117.1:p.Cys523Phe
NM_004518.5:c.1484G>T	NP_004509.2:p.Cys495Phe
NM_172106.2:c.1514G>T	NP_742104.1:p.Cys505Phe
NM_172107.3:c.1568G>T	NP_742105.1:p.Cys523Phe
NM_172108.4:c.1475G>T	NP_742106.1:p.Cys492Phe
XM_011528810.2:c.1514G>T	XP_011527112.1:p.Cys505Phe
XM_011528811.2:c.1484G>T	XP_011527113.1:p.Cys495Phe
XM_017027841.2:c.1511G>T	XP_016883330.1:p.Cys504Phe
XM_017027842.2:c.1514G>T	XP_016883331.1:p.Cys505Phe
XM_017027843.1:c.1445G>T	XP_016883332.1:p.Cys482Phe
XM_017027844.2:c.1511G>T	XP_016883333.1:p.Cys504Phe
XM_017027845.1:c.476G>T	XP_016883334.1:p.Cys159Phe
NM_004518.6:c.1484G>T	NP_004509.2:p.Cys495Phe
NM_172106.3:c.1514G>T	NP_742104.1:p.Cys505Phe
NM_172107.4:c.1568G>T MANE Select	NP_742105.1:p.Cys523Phe
NM_172108.5:c.1475G>T	NP_742106.1:p.Cys492Phe
NM_001382235.1:c.1514G>T	NP_001369164.1:p.Cys505Phe