Canonical Allele Identifier: CA409637361

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038231G>C (hg19) ; chr20:g.63406878G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406878G>C , CM000682.2:g.63406878G>C	GRCh38
NC_000020.10:g.62038231G>C , CM000682.1:g.62038231G>C	GRCh37
NC_000020.9:g.61508675G>C	NCBI36
NG_009004.1:g.70763C>G
NG_009004.2:g.70763C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2439C>G	ENSP00000516702.1:p.His813Gln
ENST00000359125.7:c.2385C>G MANE Select	ENSP00000352035.2:p.His795Gln
ENST00000637193.1:c.1782C>G	ENSP00000490734.1:p.His594Gln
ENST00000344462.8:c.2292C>G	ENSP00000339611.4:p.His764Gln
ENST00000357249.6:c.1953C>G	ENSP00000349789.3:p.His651Gln
ENST00000359125.6:c.2385C>G	ENSP00000352035.2:p.His795Gln
ENST00000360480.7:c.2301C>G	ENSP00000353668.3:p.His767Gln
ENST00000370224.5:c.2241+168C>G	ENSP00000359244.2:n.2241+168C>G
ENST00000625514.2:c.2205+168C>G	ENSP00000486040.1:n.2205+168C>G
ENST00000626839.2:c.2331C>G	ENSP00000486706.1:p.His777Gln
ENST00000629241.2:c.2133+168C>G	ENSP00000487142.1:n.2133+168C>G
ENST00000629676.2:c.1680-6035C>G	ENSP00000486194.1:n.1680-6035C>G
NM_004518.4:c.2301C>G	NP_004509.2:p.His767Gln
NM_172106.1:c.2331C>G	NP_742104.1:p.His777Gln
NM_172107.2:c.2385C>G	NP_742105.1:p.His795Gln
NM_172108.3:c.2292C>G	NP_742106.1:p.His764Gln
XM_006723787.1:c.2427C>G	XP_006723850.1:p.His809Gln
XM_011528807.1:c.2493C>G	XP_011527109.1:p.His831Gln
XM_011528808.1:c.2490C>G	XP_011527110.1:p.His830Gln
XM_011528809.1:c.2463C>G	XP_011527111.1:p.His821Gln
XM_011528810.1:c.2439C>G	XP_011527112.1:p.His813Gln
XM_011528811.1:c.2409C>G	XP_011527113.1:p.His803Gln
XM_011528812.1:c.2382C>G	XP_011527114.1:p.His794Gln
XM_011528813.1:c.2367C>G	XP_011527115.1:p.His789Gln
XM_011528814.1:c.1974C>G	XP_011527116.1:p.His658Gln
NM_004518.5:c.2301C>G	NP_004509.2:p.His767Gln
NM_172106.2:c.2331C>G	NP_742104.1:p.His777Gln
NM_172107.3:c.2385C>G	NP_742105.1:p.His795Gln
NM_172108.4:c.2292C>G	NP_742106.1:p.His764Gln
XM_011528810.2:c.2439C>G	XP_011527112.1:p.His813Gln
XM_011528811.2:c.2409C>G	XP_011527113.1:p.His803Gln
XM_017027841.2:c.2436C>G	XP_016883330.1:p.His812Gln
XM_017027842.2:c.2373C>G	XP_016883331.1:p.His791Gln
XM_017027843.1:c.2370C>G	XP_016883332.1:p.His790Gln
XM_017027844.2:c.2328C>G	XP_016883333.1:p.His776Gln
XM_017027845.1:c.1401C>G	XP_016883334.1:p.His467Gln
NM_004518.6:c.2301C>G	NP_004509.2:p.His767Gln
NM_172106.3:c.2331C>G	NP_742104.1:p.His777Gln
NM_172107.4:c.2385C>G MANE Select	NP_742105.1:p.His795Gln
NM_172108.5:c.2292C>G	NP_742106.1:p.His764Gln
NM_001382235.1:c.2439C>G	NP_001369164.1:p.His813Gln