Canonical Allele Identifier: CA409637734

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038287G>T (hg19) ; chr20:g.63406934G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406934G>T , CM000682.2:g.63406934G>T	GRCh38
NC_000020.10:g.62038287G>T , CM000682.1:g.62038287G>T	GRCh37
NC_000020.9:g.61508731G>T	NCBI36
NG_009004.1:g.70707C>A
NG_009004.2:g.70707C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2383C>A	ENSP00000516702.1:p.Pro795Thr
ENST00000359125.7:c.2329C>A MANE Select	ENSP00000352035.2:p.Pro777Thr
ENST00000637193.1:c.1726C>A	ENSP00000490734.1:p.Pro576Thr
ENST00000344462.8:c.2236C>A	ENSP00000339611.4:p.Pro746Thr
ENST00000357249.6:c.1897C>A	ENSP00000349789.3:p.Pro633Thr
ENST00000359125.6:c.2329C>A	ENSP00000352035.2:p.Pro777Thr
ENST00000360480.7:c.2245C>A	ENSP00000353668.3:p.Pro749Thr
ENST00000370224.5:c.2241+112C>A	ENSP00000359244.2:n.2241+112C>A
ENST00000625514.2:c.2205+112C>A	ENSP00000486040.1:n.2205+112C>A
ENST00000626839.2:c.2275C>A	ENSP00000486706.1:p.Pro759Thr
ENST00000629241.2:c.2133+112C>A	ENSP00000487142.1:n.2133+112C>A
ENST00000629676.2:c.1680-6091C>A	ENSP00000486194.1:n.1680-6091C>A
NM_004518.4:c.2245C>A	NP_004509.2:p.Pro749Thr
NM_172106.1:c.2275C>A	NP_742104.1:p.Pro759Thr
NM_172107.2:c.2329C>A	NP_742105.1:p.Pro777Thr
NM_172108.3:c.2236C>A	NP_742106.1:p.Pro746Thr
XM_006723787.1:c.2371C>A	XP_006723850.1:p.Pro791Thr
XM_011528807.1:c.2437C>A	XP_011527109.1:p.Pro813Thr
XM_011528808.1:c.2434C>A	XP_011527110.1:p.Pro812Thr
XM_011528809.1:c.2407C>A	XP_011527111.1:p.Pro803Thr
XM_011528810.1:c.2383C>A	XP_011527112.1:p.Pro795Thr
XM_011528811.1:c.2353C>A	XP_011527113.1:p.Pro785Thr
XM_011528812.1:c.2326C>A	XP_011527114.1:p.Pro776Thr
XM_011528813.1:c.2311C>A	XP_011527115.1:p.Pro771Thr
XM_011528814.1:c.1918C>A	XP_011527116.1:p.Pro640Thr
NM_004518.5:c.2245C>A	NP_004509.2:p.Pro749Thr
NM_172106.2:c.2275C>A	NP_742104.1:p.Pro759Thr
NM_172107.3:c.2329C>A	NP_742105.1:p.Pro777Thr
NM_172108.4:c.2236C>A	NP_742106.1:p.Pro746Thr
XM_011528810.2:c.2383C>A	XP_011527112.1:p.Pro795Thr
XM_011528811.2:c.2353C>A	XP_011527113.1:p.Pro785Thr
XM_017027841.2:c.2380C>A	XP_016883330.1:p.Pro794Thr
XM_017027842.2:c.2317C>A	XP_016883331.1:p.Pro773Thr
XM_017027843.1:c.2314C>A	XP_016883332.1:p.Pro772Thr
XM_017027844.2:c.2272C>A	XP_016883333.1:p.Pro758Thr
XM_017027845.1:c.1345C>A	XP_016883334.1:p.Pro449Thr
NM_004518.6:c.2245C>A	NP_004509.2:p.Pro749Thr
NM_172106.3:c.2275C>A	NP_742104.1:p.Pro759Thr
NM_172107.4:c.2329C>A MANE Select	NP_742105.1:p.Pro777Thr
NM_172108.5:c.2236C>A	NP_742106.1:p.Pro746Thr
NM_001382235.1:c.2383C>A	NP_001369164.1:p.Pro795Thr