Canonical Allele Identifier: CA409637014

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038163T>G (hg19) ; chr20:g.63406810T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406810T>G , CM000682.2:g.63406810T>G	GRCh38
NC_000020.10:g.62038163T>G , CM000682.1:g.62038163T>G	GRCh37
NC_000020.9:g.61508607T>G	NCBI36
NG_009004.1:g.70831A>C
NG_009004.2:g.70831A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2507A>C	ENSP00000516702.1:p.Asn836Thr
ENST00000359125.7:c.2453A>C MANE Select	ENSP00000352035.2:p.Asn818Thr
ENST00000637193.1:c.1850A>C	ENSP00000490734.1:p.Asn617Thr
ENST00000344462.8:c.2360A>C	ENSP00000339611.4:p.Asn787Thr
ENST00000357249.6:c.2021A>C	ENSP00000349789.3:p.Asn674Thr
ENST00000359125.6:c.2453A>C	ENSP00000352035.2:p.Asn818Thr
ENST00000360480.7:c.2369A>C	ENSP00000353668.3:p.Asn790Thr
ENST00000370224.5:c.2241+236A>C	ENSP00000359244.2:n.2241+236A>C
ENST00000625514.2:c.2205+236A>C	ENSP00000486040.1:n.2205+236A>C
ENST00000626839.2:c.2399A>C	ENSP00000486706.1:p.Asn800Thr
ENST00000629241.2:c.2133+236A>C	ENSP00000487142.1:n.2133+236A>C
ENST00000629676.2:c.1680-5967A>C	ENSP00000486194.1:n.1680-5967A>C
NM_004518.4:c.2369A>C	NP_004509.2:p.Asn790Thr
NM_172106.1:c.2399A>C	NP_742104.1:p.Asn800Thr
NM_172107.2:c.2453A>C	NP_742105.1:p.Asn818Thr
NM_172108.3:c.2360A>C	NP_742106.1:p.Asn787Thr
XM_006723787.1:c.2495A>C	XP_006723850.1:p.Asn832Thr
XM_011528807.1:c.2561A>C	XP_011527109.1:p.Asn854Thr
XM_011528808.1:c.2558A>C	XP_011527110.1:p.Asn853Thr
XM_011528809.1:c.2531A>C	XP_011527111.1:p.Asn844Thr
XM_011528810.1:c.2507A>C	XP_011527112.1:p.Asn836Thr
XM_011528811.1:c.2477A>C	XP_011527113.1:p.Asn826Thr
XM_011528812.1:c.2450A>C	XP_011527114.1:p.Asn817Thr
XM_011528813.1:c.2435A>C	XP_011527115.1:p.Asn812Thr
XM_011528814.1:c.2042A>C	XP_011527116.1:p.Asn681Thr
NM_004518.5:c.2369A>C	NP_004509.2:p.Asn790Thr
NM_172106.2:c.2399A>C	NP_742104.1:p.Asn800Thr
NM_172107.3:c.2453A>C	NP_742105.1:p.Asn818Thr
NM_172108.4:c.2360A>C	NP_742106.1:p.Asn787Thr
XM_011528810.2:c.2507A>C	XP_011527112.1:p.Asn836Thr
XM_011528811.2:c.2477A>C	XP_011527113.1:p.Asn826Thr
XM_017027841.2:c.2504A>C	XP_016883330.1:p.Asn835Thr
XM_017027842.2:c.2441A>C	XP_016883331.1:p.Asn814Thr
XM_017027843.1:c.2438A>C	XP_016883332.1:p.Asn813Thr
XM_017027844.2:c.2396A>C	XP_016883333.1:p.Asn799Thr
XM_017027845.1:c.1469A>C	XP_016883334.1:p.Asn490Thr
NM_004518.6:c.2369A>C	NP_004509.2:p.Asn790Thr
NM_172106.3:c.2399A>C	NP_742104.1:p.Asn800Thr
NM_172107.4:c.2453A>C MANE Select	NP_742105.1:p.Asn818Thr
NM_172108.5:c.2360A>C	NP_742106.1:p.Asn787Thr
NM_001382235.1:c.2507A>C	NP_001369164.1:p.Asn836Thr