Canonical Allele Identifier: CA511339188

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038036A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406683A>C , CM000682.2:g.63406683A>C	GRCh38
NC_000020.10:g.62038036A>C , CM000682.1:g.62038036A>C	GRCh37
NC_000020.9:g.61508480A>C	NCBI36
NG_009004.1:g.70958T>G
NG_009004.2:g.70958T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2634T>G	ENSP00000516702.1:p.Gly878=
ENST00000359125.7:c.2580T>G MANE Select	ENSP00000352035.2:p.Gly860=
ENST00000637193.1:c.1977T>G	ENSP00000490734.1:p.Gly659=
ENST00000344462.8:c.2487T>G	ENSP00000339611.4:p.Gly829=
ENST00000357249.6:c.2148T>G	ENSP00000349789.3:p.Gly716=
ENST00000359125.6:c.2580T>G	ENSP00000352035.2:p.Gly860=
ENST00000360480.7:c.2496T>G	ENSP00000353668.3:p.Gly832=
ENST00000370224.5:c.2241+363T>G	ENSP00000359244.2:n.2241+363T>G
ENST00000625514.2:c.2205+363T>G	ENSP00000486040.1:n.2205+363T>G
ENST00000626839.2:c.2526T>G	ENSP00000486706.1:p.Gly842=
ENST00000629241.2:c.2133+363T>G	ENSP00000487142.1:n.2133+363T>G
ENST00000629676.2:c.1680-5840T>G	ENSP00000486194.1:n.1680-5840T>G
NM_004518.4:c.2496T>G	NP_004509.2:p.Gly832=
NM_172106.1:c.2526T>G	NP_742104.1:p.Gly842=
NM_172107.2:c.2580T>G	NP_742105.1:p.Gly860=
NM_172108.3:c.2487T>G	NP_742106.1:p.Gly829=
XM_006723787.1:c.2622T>G	XP_006723850.1:p.Gly874=
XM_011528807.1:c.2688T>G	XP_011527109.1:p.Gly896=
XM_011528808.1:c.2685T>G	XP_011527110.1:p.Gly895=
XM_011528809.1:c.2658T>G	XP_011527111.1:p.Gly886=
XM_011528810.1:c.2634T>G	XP_011527112.1:p.Gly878=
XM_011528811.1:c.2604T>G	XP_011527113.1:p.Gly868=
XM_011528812.1:c.2577T>G	XP_011527114.1:p.Gly859=
XM_011528813.1:c.2562T>G	XP_011527115.1:p.Gly854=
XM_011528814.1:c.2169T>G	XP_011527116.1:p.Gly723=
NM_004518.5:c.2496T>G	NP_004509.2:p.Gly832=
NM_172106.2:c.2526T>G	NP_742104.1:p.Gly842=
NM_172107.3:c.2580T>G	NP_742105.1:p.Gly860=
NM_172108.4:c.2487T>G	NP_742106.1:p.Gly829=
XM_011528810.2:c.2634T>G	XP_011527112.1:p.Gly878=
XM_011528811.2:c.2604T>G	XP_011527113.1:p.Gly868=
XM_017027841.2:c.2631T>G	XP_016883330.1:p.Gly877=
XM_017027842.2:c.2568T>G	XP_016883331.1:p.Gly856=
XM_017027843.1:c.2565T>G	XP_016883332.1:p.Gly855=
XM_017027844.2:c.2523T>G	XP_016883333.1:p.Gly841=
XM_017027845.1:c.1596T>G	XP_016883334.1:p.Gly532=
NM_004518.6:c.2496T>G	NP_004509.2:p.Gly832=
NM_172106.3:c.2526T>G	NP_742104.1:p.Gly842=
NM_172107.4:c.2580T>G MANE Select	NP_742105.1:p.Gly860=
NM_172108.5:c.2487T>G	NP_742106.1:p.Gly829=
NM_001382235.1:c.2634T>G	NP_001369164.1:p.Gly878=