Canonical Allele Identifier: CA409637306

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63406871-G-T
• MyVariant Identifiers: chr20:g.62038224G>T (hg19) ; chr20:g.63406871G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406871G>T , CM000682.2:g.63406871G>T	GRCh38
NC_000020.10:g.62038224G>T , CM000682.1:g.62038224G>T	GRCh37
NC_000020.9:g.61508668G>T	NCBI36
NG_009004.1:g.70770C>A
NG_009004.2:g.70770C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2446C>A	ENSP00000516702.1:p.Leu816Met
ENST00000359125.7:c.2392C>A MANE Select	ENSP00000352035.2:p.Leu798Met
ENST00000637193.1:c.1789C>A	ENSP00000490734.1:p.Leu597Met
ENST00000344462.8:c.2299C>A	ENSP00000339611.4:p.Leu767Met
ENST00000357249.6:c.1960C>A	ENSP00000349789.3:p.Leu654Met
ENST00000359125.6:c.2392C>A	ENSP00000352035.2:p.Leu798Met
ENST00000360480.7:c.2308C>A	ENSP00000353668.3:p.Leu770Met
ENST00000370224.5:c.2241+175C>A	ENSP00000359244.2:n.2241+175C>A
ENST00000625514.2:c.2205+175C>A	ENSP00000486040.1:n.2205+175C>A
ENST00000626839.2:c.2338C>A	ENSP00000486706.1:p.Leu780Met
ENST00000629241.2:c.2133+175C>A	ENSP00000487142.1:n.2133+175C>A
ENST00000629676.2:c.1680-6028C>A	ENSP00000486194.1:n.1680-6028C>A
NM_004518.4:c.2308C>A	NP_004509.2:p.Leu770Met
NM_172106.1:c.2338C>A	NP_742104.1:p.Leu780Met
NM_172107.2:c.2392C>A	NP_742105.1:p.Leu798Met
NM_172108.3:c.2299C>A	NP_742106.1:p.Leu767Met
XM_006723787.1:c.2434C>A	XP_006723850.1:p.Leu812Met
XM_011528807.1:c.2500C>A	XP_011527109.1:p.Leu834Met
XM_011528808.1:c.2497C>A	XP_011527110.1:p.Leu833Met
XM_011528809.1:c.2470C>A	XP_011527111.1:p.Leu824Met
XM_011528810.1:c.2446C>A	XP_011527112.1:p.Leu816Met
XM_011528811.1:c.2416C>A	XP_011527113.1:p.Leu806Met
XM_011528812.1:c.2389C>A	XP_011527114.1:p.Leu797Met
XM_011528813.1:c.2374C>A	XP_011527115.1:p.Leu792Met
XM_011528814.1:c.1981C>A	XP_011527116.1:p.Leu661Met
NM_004518.5:c.2308C>A	NP_004509.2:p.Leu770Met
NM_172106.2:c.2338C>A	NP_742104.1:p.Leu780Met
NM_172107.3:c.2392C>A	NP_742105.1:p.Leu798Met
NM_172108.4:c.2299C>A	NP_742106.1:p.Leu767Met
XM_011528810.2:c.2446C>A	XP_011527112.1:p.Leu816Met
XM_011528811.2:c.2416C>A	XP_011527113.1:p.Leu806Met
XM_017027841.2:c.2443C>A	XP_016883330.1:p.Leu815Met
XM_017027842.2:c.2380C>A	XP_016883331.1:p.Leu794Met
XM_017027843.1:c.2377C>A	XP_016883332.1:p.Leu793Met
XM_017027844.2:c.2335C>A	XP_016883333.1:p.Leu779Met
XM_017027845.1:c.1408C>A	XP_016883334.1:p.Leu470Met
NM_004518.6:c.2308C>A	NP_004509.2:p.Leu770Met
NM_172106.3:c.2338C>A	NP_742104.1:p.Leu780Met
NM_172107.4:c.2392C>A MANE Select	NP_742105.1:p.Leu798Met
NM_172108.5:c.2299C>A	NP_742106.1:p.Leu767Met
NM_001382235.1:c.2446C>A	NP_001369164.1:p.Leu816Met