Canonical Allele Identifier: CA511339351

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038168A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406815A>T , CM000682.2:g.63406815A>T	GRCh38
NC_000020.10:g.62038168A>T , CM000682.1:g.62038168A>T	GRCh37
NC_000020.9:g.61508612A>T	NCBI36
NG_009004.1:g.70826T>A
NG_009004.2:g.70826T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2502T>A	ENSP00000516702.1:p.Ala834=
ENST00000359125.7:c.2448T>A MANE Select	ENSP00000352035.2:p.Ala816=
ENST00000637193.1:c.1845T>A	ENSP00000490734.1:p.Ala615=
ENST00000344462.8:c.2355T>A	ENSP00000339611.4:p.Ala785=
ENST00000357249.6:c.2016T>A	ENSP00000349789.3:p.Ala672=
ENST00000359125.6:c.2448T>A	ENSP00000352035.2:p.Ala816=
ENST00000360480.7:c.2364T>A	ENSP00000353668.3:p.Ala788=
ENST00000370224.5:c.2241+231T>A	ENSP00000359244.2:n.2241+231T>A
ENST00000625514.2:c.2205+231T>A	ENSP00000486040.1:n.2205+231T>A
ENST00000626839.2:c.2394T>A	ENSP00000486706.1:p.Ala798=
ENST00000629241.2:c.2133+231T>A	ENSP00000487142.1:n.2133+231T>A
ENST00000629676.2:c.1680-5972T>A	ENSP00000486194.1:n.1680-5972T>A
NM_004518.4:c.2364T>A	NP_004509.2:p.Ala788=
NM_172106.1:c.2394T>A	NP_742104.1:p.Ala798=
NM_172107.2:c.2448T>A	NP_742105.1:p.Ala816=
NM_172108.3:c.2355T>A	NP_742106.1:p.Ala785=
XM_006723787.1:c.2490T>A	XP_006723850.1:p.Ala830=
XM_011528807.1:c.2556T>A	XP_011527109.1:p.Ala852=
XM_011528808.1:c.2553T>A	XP_011527110.1:p.Ala851=
XM_011528809.1:c.2526T>A	XP_011527111.1:p.Ala842=
XM_011528810.1:c.2502T>A	XP_011527112.1:p.Ala834=
XM_011528811.1:c.2472T>A	XP_011527113.1:p.Ala824=
XM_011528812.1:c.2445T>A	XP_011527114.1:p.Ala815=
XM_011528813.1:c.2430T>A	XP_011527115.1:p.Ala810=
XM_011528814.1:c.2037T>A	XP_011527116.1:p.Ala679=
NM_004518.5:c.2364T>A	NP_004509.2:p.Ala788=
NM_172106.2:c.2394T>A	NP_742104.1:p.Ala798=
NM_172107.3:c.2448T>A	NP_742105.1:p.Ala816=
NM_172108.4:c.2355T>A	NP_742106.1:p.Ala785=
XM_011528810.2:c.2502T>A	XP_011527112.1:p.Ala834=
XM_011528811.2:c.2472T>A	XP_011527113.1:p.Ala824=
XM_017027841.2:c.2499T>A	XP_016883330.1:p.Ala833=
XM_017027842.2:c.2436T>A	XP_016883331.1:p.Ala812=
XM_017027843.1:c.2433T>A	XP_016883332.1:p.Ala811=
XM_017027844.2:c.2391T>A	XP_016883333.1:p.Ala797=
XM_017027845.1:c.1464T>A	XP_016883334.1:p.Ala488=
NM_004518.6:c.2364T>A	NP_004509.2:p.Ala788=
NM_172106.3:c.2394T>A	NP_742104.1:p.Ala798=
NM_172107.4:c.2448T>A MANE Select	NP_742105.1:p.Ala816=
NM_172108.5:c.2355T>A	NP_742106.1:p.Ala785=
NM_001382235.1:c.2502T>A	NP_001369164.1:p.Ala834=