Canonical Allele Identifier: CA409639016

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 1361264
• ClinVar RCV Id: RCV001874280
• dbSNP Id: rs1398433237
• gnomAD v4: 20-63407173-C-T
• COSMIC: COSM1413090 ; COSM4786035 ; COSM4786036
• MyVariant Identifiers: chr20:g.62038526C>T (hg19) ; chr20:g.63407173C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407173C>T , CM000682.2:g.63407173C>T	GRCh38
NC_000020.10:g.62038526C>T , CM000682.1:g.62038526C>T	GRCh37
NC_000020.9:g.61508970C>T	NCBI36
NG_009004.1:g.70468G>A
NG_009004.2:g.70468G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2144G>A	ENSP00000516702.1:p.Gly715Asp
ENST00000359125.7:c.2090G>A MANE Select	ENSP00000352035.2:p.Gly697Asp
ENST00000637193.1:c.1487G>A	ENSP00000490734.1:p.Gly496Asp
ENST00000344462.8:c.1997G>A	ENSP00000339611.4:p.Gly666Asp
ENST00000357249.6:c.1658G>A	ENSP00000349789.3:p.Gly553Asp
ENST00000359125.6:c.2090G>A	ENSP00000352035.2:p.Gly697Asp
ENST00000360480.7:c.2006G>A	ENSP00000353668.3:p.Gly669Asp
ENST00000370224.5:c.2114G>A	ENSP00000359244.2:p.Gly705Asp
ENST00000625514.2:c.2078G>A	ENSP00000486040.1:p.Gly693Asp
ENST00000626839.2:c.2036G>A	ENSP00000486706.1:p.Gly679Asp
ENST00000629241.2:c.2006G>A	ENSP00000487142.1:p.Gly669Asp
ENST00000629676.2:c.1679+6277G>A	ENSP00000486194.1:n.1679+6277G>A
NM_004518.4:c.2006G>A	NP_004509.2:p.Gly669Asp
NM_172106.1:c.2036G>A	NP_742104.1:p.Gly679Asp
NM_172107.2:c.2090G>A	NP_742105.1:p.Gly697Asp
NM_172108.3:c.1997G>A	NP_742106.1:p.Gly666Asp
XM_006723787.1:c.2132G>A	XP_006723850.1:p.Gly711Asp
XM_011528807.1:c.2198G>A	XP_011527109.1:p.Gly733Asp
XM_011528808.1:c.2195G>A	XP_011527110.1:p.Gly732Asp
XM_011528809.1:c.2168G>A	XP_011527111.1:p.Gly723Asp
XM_011528810.1:c.2144G>A	XP_011527112.1:p.Gly715Asp
XM_011528811.1:c.2114G>A	XP_011527113.1:p.Gly705Asp
XM_011528812.1:c.2087G>A	XP_011527114.1:p.Gly696Asp
XM_011528813.1:c.2072G>A	XP_011527115.1:p.Gly691Asp
XM_011528814.1:c.1679G>A	XP_011527116.1:p.Gly560Asp
NM_004518.5:c.2006G>A	NP_004509.2:p.Gly669Asp
NM_172106.2:c.2036G>A	NP_742104.1:p.Gly679Asp
NM_172107.3:c.2090G>A	NP_742105.1:p.Gly697Asp
NM_172108.4:c.1997G>A	NP_742106.1:p.Gly666Asp
XM_011528810.2:c.2144G>A	XP_011527112.1:p.Gly715Asp
XM_011528811.2:c.2114G>A	XP_011527113.1:p.Gly705Asp
XM_017027841.2:c.2141G>A	XP_016883330.1:p.Gly714Asp
XM_017027842.2:c.2078G>A	XP_016883331.1:p.Gly693Asp
XM_017027843.1:c.2075G>A	XP_016883332.1:p.Gly692Asp
XM_017027844.2:c.2033G>A	XP_016883333.1:p.Gly678Asp
XM_017027845.1:c.1106G>A	XP_016883334.1:p.Gly369Asp
NM_004518.6:c.2006G>A	NP_004509.2:p.Gly669Asp
NM_172106.3:c.2036G>A	NP_742104.1:p.Gly679Asp
NM_172107.4:c.2090G>A MANE Select	NP_742105.1:p.Gly697Asp
NM_172108.5:c.1997G>A	NP_742106.1:p.Gly666Asp
NM_001382235.1:c.2144G>A	NP_001369164.1:p.Gly715Asp