Canonical Allele Identifier: CA511339431

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038222C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406869C>G , CM000682.2:g.63406869C>G	GRCh38
NC_000020.10:g.62038222C>G , CM000682.1:g.62038222C>G	GRCh37
NC_000020.9:g.61508666C>G	NCBI36
NG_009004.1:g.70772G>C
NG_009004.2:g.70772G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2448G>C	ENSP00000516702.1:p.Leu816=
ENST00000359125.7:c.2394G>C MANE Select	ENSP00000352035.2:p.Leu798=
ENST00000637193.1:c.1791G>C	ENSP00000490734.1:p.Leu597=
ENST00000344462.8:c.2301G>C	ENSP00000339611.4:p.Leu767=
ENST00000357249.6:c.1962G>C	ENSP00000349789.3:p.Leu654=
ENST00000359125.6:c.2394G>C	ENSP00000352035.2:p.Leu798=
ENST00000360480.7:c.2310G>C	ENSP00000353668.3:p.Leu770=
ENST00000370224.5:c.2241+177G>C	ENSP00000359244.2:n.2241+177G>C
ENST00000625514.2:c.2205+177G>C	ENSP00000486040.1:n.2205+177G>C
ENST00000626839.2:c.2340G>C	ENSP00000486706.1:p.Leu780=
ENST00000629241.2:c.2133+177G>C	ENSP00000487142.1:n.2133+177G>C
ENST00000629676.2:c.1680-6026G>C	ENSP00000486194.1:n.1680-6026G>C
NM_004518.4:c.2310G>C	NP_004509.2:p.Leu770=
NM_172106.1:c.2340G>C	NP_742104.1:p.Leu780=
NM_172107.2:c.2394G>C	NP_742105.1:p.Leu798=
NM_172108.3:c.2301G>C	NP_742106.1:p.Leu767=
XM_006723787.1:c.2436G>C	XP_006723850.1:p.Leu812=
XM_011528807.1:c.2502G>C	XP_011527109.1:p.Leu834=
XM_011528808.1:c.2499G>C	XP_011527110.1:p.Leu833=
XM_011528809.1:c.2472G>C	XP_011527111.1:p.Leu824=
XM_011528810.1:c.2448G>C	XP_011527112.1:p.Leu816=
XM_011528811.1:c.2418G>C	XP_011527113.1:p.Leu806=
XM_011528812.1:c.2391G>C	XP_011527114.1:p.Leu797=
XM_011528813.1:c.2376G>C	XP_011527115.1:p.Leu792=
XM_011528814.1:c.1983G>C	XP_011527116.1:p.Leu661=
NM_004518.5:c.2310G>C	NP_004509.2:p.Leu770=
NM_172106.2:c.2340G>C	NP_742104.1:p.Leu780=
NM_172107.3:c.2394G>C	NP_742105.1:p.Leu798=
NM_172108.4:c.2301G>C	NP_742106.1:p.Leu767=
XM_011528810.2:c.2448G>C	XP_011527112.1:p.Leu816=
XM_011528811.2:c.2418G>C	XP_011527113.1:p.Leu806=
XM_017027841.2:c.2445G>C	XP_016883330.1:p.Leu815=
XM_017027842.2:c.2382G>C	XP_016883331.1:p.Leu794=
XM_017027843.1:c.2379G>C	XP_016883332.1:p.Leu793=
XM_017027844.2:c.2337G>C	XP_016883333.1:p.Leu779=
XM_017027845.1:c.1410G>C	XP_016883334.1:p.Leu470=
NM_004518.6:c.2310G>C	NP_004509.2:p.Leu770=
NM_172106.3:c.2340G>C	NP_742104.1:p.Leu780=
NM_172107.4:c.2394G>C MANE Select	NP_742105.1:p.Leu798=
NM_172108.5:c.2301G>C	NP_742106.1:p.Leu767=
NM_001382235.1:c.2448G>C	NP_001369164.1:p.Leu816=