Canonical Allele Identifier: CA409637467

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63406895-T-C
• MyVariant Identifiers: chr20:g.62038248T>C (hg19) ; chr20:g.63406895T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406895T>C , CM000682.2:g.63406895T>C	GRCh38
NC_000020.10:g.62038248T>C , CM000682.1:g.62038248T>C	GRCh37
NC_000020.9:g.61508692T>C	NCBI36
NG_009004.1:g.70746A>G
NG_009004.2:g.70746A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2422A>G	ENSP00000516702.1:p.Ile808Val
ENST00000359125.7:c.2368A>G MANE Select	ENSP00000352035.2:p.Ile790Val
ENST00000637193.1:c.1765A>G	ENSP00000490734.1:p.Ile589Val
ENST00000344462.8:c.2275A>G	ENSP00000339611.4:p.Ile759Val
ENST00000357249.6:c.1936A>G	ENSP00000349789.3:p.Ile646Val
ENST00000359125.6:c.2368A>G	ENSP00000352035.2:p.Ile790Val
ENST00000360480.7:c.2284A>G	ENSP00000353668.3:p.Ile762Val
ENST00000370224.5:c.2241+151A>G	ENSP00000359244.2:n.2241+151A>G
ENST00000625514.2:c.2205+151A>G	ENSP00000486040.1:n.2205+151A>G
ENST00000626839.2:c.2314A>G	ENSP00000486706.1:p.Ile772Val
ENST00000629241.2:c.2133+151A>G	ENSP00000487142.1:n.2133+151A>G
ENST00000629676.2:c.1680-6052A>G	ENSP00000486194.1:n.1680-6052A>G
NM_004518.4:c.2284A>G	NP_004509.2:p.Ile762Val
NM_172106.1:c.2314A>G	NP_742104.1:p.Ile772Val
NM_172107.2:c.2368A>G	NP_742105.1:p.Ile790Val
NM_172108.3:c.2275A>G	NP_742106.1:p.Ile759Val
XM_006723787.1:c.2410A>G	XP_006723850.1:p.Ile804Val
XM_011528807.1:c.2476A>G	XP_011527109.1:p.Ile826Val
XM_011528808.1:c.2473A>G	XP_011527110.1:p.Ile825Val
XM_011528809.1:c.2446A>G	XP_011527111.1:p.Ile816Val
XM_011528810.1:c.2422A>G	XP_011527112.1:p.Ile808Val
XM_011528811.1:c.2392A>G	XP_011527113.1:p.Ile798Val
XM_011528812.1:c.2365A>G	XP_011527114.1:p.Ile789Val
XM_011528813.1:c.2350A>G	XP_011527115.1:p.Ile784Val
XM_011528814.1:c.1957A>G	XP_011527116.1:p.Ile653Val
NM_004518.5:c.2284A>G	NP_004509.2:p.Ile762Val
NM_172106.2:c.2314A>G	NP_742104.1:p.Ile772Val
NM_172107.3:c.2368A>G	NP_742105.1:p.Ile790Val
NM_172108.4:c.2275A>G	NP_742106.1:p.Ile759Val
XM_011528810.2:c.2422A>G	XP_011527112.1:p.Ile808Val
XM_011528811.2:c.2392A>G	XP_011527113.1:p.Ile798Val
XM_017027841.2:c.2419A>G	XP_016883330.1:p.Ile807Val
XM_017027842.2:c.2356A>G	XP_016883331.1:p.Ile786Val
XM_017027843.1:c.2353A>G	XP_016883332.1:p.Ile785Val
XM_017027844.2:c.2311A>G	XP_016883333.1:p.Ile771Val
XM_017027845.1:c.1384A>G	XP_016883334.1:p.Ile462Val
NM_004518.6:c.2284A>G	NP_004509.2:p.Ile762Val
NM_172106.3:c.2314A>G	NP_742104.1:p.Ile772Val
NM_172107.4:c.2368A>G MANE Select	NP_742105.1:p.Ile790Val
NM_172108.5:c.2275A>G	NP_742106.1:p.Ile759Val
NM_001382235.1:c.2422A>G	NP_001369164.1:p.Ile808Val