Canonical Allele Identifier: CA409637649

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038274A>C (hg19) ; chr20:g.63406921A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406921A>C , CM000682.2:g.63406921A>C	GRCh38
NC_000020.10:g.62038274A>C , CM000682.1:g.62038274A>C	GRCh37
NC_000020.9:g.61508718A>C	NCBI36
NG_009004.1:g.70720T>G
NG_009004.2:g.70720T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2396T>G	ENSP00000516702.1:p.Leu799Arg
ENST00000359125.7:c.2342T>G MANE Select	ENSP00000352035.2:p.Leu781Arg
ENST00000637193.1:c.1739T>G	ENSP00000490734.1:p.Leu580Arg
ENST00000344462.8:c.2249T>G	ENSP00000339611.4:p.Leu750Arg
ENST00000357249.6:c.1910T>G	ENSP00000349789.3:p.Leu637Arg
ENST00000359125.6:c.2342T>G	ENSP00000352035.2:p.Leu781Arg
ENST00000360480.7:c.2258T>G	ENSP00000353668.3:p.Leu753Arg
ENST00000370224.5:c.2241+125T>G	ENSP00000359244.2:n.2241+125T>G
ENST00000625514.2:c.2205+125T>G	ENSP00000486040.1:n.2205+125T>G
ENST00000626839.2:c.2288T>G	ENSP00000486706.1:p.Leu763Arg
ENST00000629241.2:c.2133+125T>G	ENSP00000487142.1:n.2133+125T>G
ENST00000629676.2:c.1680-6078T>G	ENSP00000486194.1:n.1680-6078T>G
NM_004518.4:c.2258T>G	NP_004509.2:p.Leu753Arg
NM_172106.1:c.2288T>G	NP_742104.1:p.Leu763Arg
NM_172107.2:c.2342T>G	NP_742105.1:p.Leu781Arg
NM_172108.3:c.2249T>G	NP_742106.1:p.Leu750Arg
XM_006723787.1:c.2384T>G	XP_006723850.1:p.Leu795Arg
XM_011528807.1:c.2450T>G	XP_011527109.1:p.Leu817Arg
XM_011528808.1:c.2447T>G	XP_011527110.1:p.Leu816Arg
XM_011528809.1:c.2420T>G	XP_011527111.1:p.Leu807Arg
XM_011528810.1:c.2396T>G	XP_011527112.1:p.Leu799Arg
XM_011528811.1:c.2366T>G	XP_011527113.1:p.Leu789Arg
XM_011528812.1:c.2339T>G	XP_011527114.1:p.Leu780Arg
XM_011528813.1:c.2324T>G	XP_011527115.1:p.Leu775Arg
XM_011528814.1:c.1931T>G	XP_011527116.1:p.Leu644Arg
NM_004518.5:c.2258T>G	NP_004509.2:p.Leu753Arg
NM_172106.2:c.2288T>G	NP_742104.1:p.Leu763Arg
NM_172107.3:c.2342T>G	NP_742105.1:p.Leu781Arg
NM_172108.4:c.2249T>G	NP_742106.1:p.Leu750Arg
XM_011528810.2:c.2396T>G	XP_011527112.1:p.Leu799Arg
XM_011528811.2:c.2366T>G	XP_011527113.1:p.Leu789Arg
XM_017027841.2:c.2393T>G	XP_016883330.1:p.Leu798Arg
XM_017027842.2:c.2330T>G	XP_016883331.1:p.Leu777Arg
XM_017027843.1:c.2327T>G	XP_016883332.1:p.Leu776Arg
XM_017027844.2:c.2285T>G	XP_016883333.1:p.Leu762Arg
XM_017027845.1:c.1358T>G	XP_016883334.1:p.Leu453Arg
NM_004518.6:c.2258T>G	NP_004509.2:p.Leu753Arg
NM_172106.3:c.2288T>G	NP_742104.1:p.Leu763Arg
NM_172107.4:c.2342T>G MANE Select	NP_742105.1:p.Leu781Arg
NM_172108.5:c.2249T>G	NP_742106.1:p.Leu750Arg
NM_001382235.1:c.2396T>G	NP_001369164.1:p.Leu799Arg