Canonical Allele Identifier: CA409636953

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038149C>T (hg19) ; chr20:g.63406796C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406796C>T , CM000682.2:g.63406796C>T	GRCh38
NC_000020.10:g.62038149C>T , CM000682.1:g.62038149C>T	GRCh37
NC_000020.9:g.61508593C>T	NCBI36
NG_009004.1:g.70845G>A
NG_009004.2:g.70845G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2521G>A	ENSP00000516702.1:p.Ala841Thr
ENST00000359125.7:c.2467G>A MANE Select	ENSP00000352035.2:p.Ala823Thr
ENST00000637193.1:c.1864G>A	ENSP00000490734.1:p.Ala622Thr
ENST00000344462.8:c.2374G>A	ENSP00000339611.4:p.Ala792Thr
ENST00000357249.6:c.2035G>A	ENSP00000349789.3:p.Ala679Thr
ENST00000359125.6:c.2467G>A	ENSP00000352035.2:p.Ala823Thr
ENST00000360480.7:c.2383G>A	ENSP00000353668.3:p.Ala795Thr
ENST00000370224.5:c.2241+250G>A	ENSP00000359244.2:n.2241+250G>A
ENST00000625514.2:c.2205+250G>A	ENSP00000486040.1:n.2205+250G>A
ENST00000626839.2:c.2413G>A	ENSP00000486706.1:p.Ala805Thr
ENST00000629241.2:c.2133+250G>A	ENSP00000487142.1:n.2133+250G>A
ENST00000629676.2:c.1680-5953G>A	ENSP00000486194.1:n.1680-5953G>A
NM_004518.4:c.2383G>A	NP_004509.2:p.Ala795Thr
NM_172106.1:c.2413G>A	NP_742104.1:p.Ala805Thr
NM_172107.2:c.2467G>A	NP_742105.1:p.Ala823Thr
NM_172108.3:c.2374G>A	NP_742106.1:p.Ala792Thr
XM_006723787.1:c.2509G>A	XP_006723850.1:p.Ala837Thr
XM_011528807.1:c.2575G>A	XP_011527109.1:p.Ala859Thr
XM_011528808.1:c.2572G>A	XP_011527110.1:p.Ala858Thr
XM_011528809.1:c.2545G>A	XP_011527111.1:p.Ala849Thr
XM_011528810.1:c.2521G>A	XP_011527112.1:p.Ala841Thr
XM_011528811.1:c.2491G>A	XP_011527113.1:p.Ala831Thr
XM_011528812.1:c.2464G>A	XP_011527114.1:p.Ala822Thr
XM_011528813.1:c.2449G>A	XP_011527115.1:p.Ala817Thr
XM_011528814.1:c.2056G>A	XP_011527116.1:p.Ala686Thr
NM_004518.5:c.2383G>A	NP_004509.2:p.Ala795Thr
NM_172106.2:c.2413G>A	NP_742104.1:p.Ala805Thr
NM_172107.3:c.2467G>A	NP_742105.1:p.Ala823Thr
NM_172108.4:c.2374G>A	NP_742106.1:p.Ala792Thr
XM_011528810.2:c.2521G>A	XP_011527112.1:p.Ala841Thr
XM_011528811.2:c.2491G>A	XP_011527113.1:p.Ala831Thr
XM_017027841.2:c.2518G>A	XP_016883330.1:p.Ala840Thr
XM_017027842.2:c.2455G>A	XP_016883331.1:p.Ala819Thr
XM_017027843.1:c.2452G>A	XP_016883332.1:p.Ala818Thr
XM_017027844.2:c.2410G>A	XP_016883333.1:p.Ala804Thr
XM_017027845.1:c.1483G>A	XP_016883334.1:p.Ala495Thr
NM_004518.6:c.2383G>A	NP_004509.2:p.Ala795Thr
NM_172106.3:c.2413G>A	NP_742104.1:p.Ala805Thr
NM_172107.4:c.2467G>A MANE Select	NP_742105.1:p.Ala823Thr
NM_172108.5:c.2374G>A	NP_742106.1:p.Ala792Thr
NM_001382235.1:c.2521G>A	NP_001369164.1:p.Ala841Thr