Canonical Allele Identifier: CA342534

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 21803
• ClinVar RCV Id: RCV000678096
• dbSNP Id: rs118192209
• MyVariant Identifiers: chr20:g.62073763C>A (hg19) ; chr20:g.63442410C>A (hg38)
• PubMed: PMID:20437616 ; PMID:25960349

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63442410C>A , CM000682.2:g.63442410C>A	GRCh38
NC_000020.10:g.62073763C>A , CM000682.1:g.62073763C>A	GRCh37
NC_000020.9:g.61544207C>A	NCBI36
NG_009004.1:g.35231G>T
NG_009004.2:g.35231G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000706989.1:c.812G>T	ENSP00000516702.1:p.Gly271Val
ENST00000344425.8:c.812G>T	ENSP00000345523.5:p.Gly271Val
ENST00000359125.7:c.812G>T MANE Select	ENSP00000352035.2:p.Gly271Val
ENST00000636255.1:n.550G>T
ENST00000637193.1:c.293G>T	ENSP00000490734.1:p.Gly98Val
ENST00000344425.7:c.812G>T	ENSP00000345523.5:p.Gly271Val
ENST00000344462.8:c.812G>T	ENSP00000339611.4:p.Gly271Val
ENST00000357249.6:c.470G>T	ENSP00000349789.3:p.Gly157Val
ENST00000359125.6:c.812G>T	ENSP00000352035.2:p.Gly271Val
ENST00000360480.7:c.812G>T	ENSP00000353668.3:p.Gly271Val
ENST00000370221.3:n.938G>T
ENST00000370224.5:c.812G>T	ENSP00000359244.2:p.Gly271Val
ENST00000625514.2:c.812G>T	ENSP00000486040.1:p.Gly271Val
ENST00000626684.1:c.177G>T
ENST00000626839.2:c.812G>T	ENSP00000486706.1:p.Gly271Val
ENST00000629241.2:c.812G>T	ENSP00000487142.1:p.Gly271Val
ENST00000629498.2:c.233G>T	ENSP00000486509.1:p.Gly78Val
ENST00000629676.2:c.812G>T	ENSP00000486194.1:p.Gly271Val
ENST00000630274.2:n.637G>T
NM_004518.4:c.812G>T	NP_004509.2:p.Gly271Val
NM_172106.1:c.812G>T	NP_742104.1:p.Gly271Val
NM_172107.2:c.812G>T	NP_742105.1:p.Gly271Val
NM_172108.3:c.812G>T	NP_742106.1:p.Gly271Val
NM_172109.1:c.812G>T	NP_742107.1:p.Gly271Val
XM_006723787.1:c.812G>T	XP_006723850.1:p.Gly271Val
XM_011528807.1:c.812G>T	XP_011527109.1:p.Gly271Val
XM_011528808.1:c.812G>T	XP_011527110.1:p.Gly271Val
XM_011528809.1:c.812G>T	XP_011527111.1:p.Gly271Val
XM_011528810.1:c.812G>T	XP_011527112.1:p.Gly271Val
XM_011528811.1:c.812G>T	XP_011527113.1:p.Gly271Val
XM_011528812.1:c.812G>T	XP_011527114.1:p.Gly271Val
XM_011528813.1:c.690+2249G>T	XP_011527115.1:n.690+2249G>T
XM_011528814.1:c.293G>T	XP_011527116.1:p.Gly98Val
XM_011528815.1:c.812G>T	XP_011527117.1:p.Gly271Val
XM_011528816.1:c.812G>T	XP_011527118.1:p.Gly271Val
NM_004518.5:c.812G>T	NP_004509.2:p.Gly271Val
NM_172106.2:c.812G>T	NP_742104.1:p.Gly271Val
NM_172107.3:c.812G>T	NP_742105.1:p.Gly271Val
NM_172108.4:c.812G>T	NP_742106.1:p.Gly271Val
NM_172109.2:c.812G>T	NP_742107.1:p.Gly271Val
XM_011528810.2:c.812G>T	XP_011527112.1:p.Gly271Val
XM_011528811.2:c.812G>T	XP_011527113.1:p.Gly271Val
XM_017027841.2:c.812G>T	XP_016883330.1:p.Gly271Val
XM_017027842.2:c.812G>T	XP_016883331.1:p.Gly271Val
XM_017027843.1:c.743G>T	XP_016883332.1:p.Gly248Val
XM_017027844.2:c.812G>T	XP_016883333.1:p.Gly271Val
NM_004518.6:c.812G>T	NP_004509.2:p.Gly271Val
NM_172106.3:c.812G>T	NP_742104.1:p.Gly271Val
NM_172107.4:c.812G>T MANE Select	NP_742105.1:p.Gly271Val
NM_172108.5:c.812G>T	NP_742106.1:p.Gly271Val
NM_172109.3:c.812G>T	NP_742107.1:p.Gly271Val
NM_001382235.1:c.812G>T	NP_001369164.1:p.Gly271Val