Canonical Allele Identifier: CA9958447

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 855445
• ClinVar RCV Id: RCV001060721
• dbSNP Id: rs540103798
• ExAC: 20:62046277 C / T
• gnomAD v2: 20-62046277-C-T
• gnomAD v3: 20-63414924-C-T
• gnomAD v4: 20-63414924-C-T
• MyVariant Identifiers: chr20:g.62046277C>T (hg19) ; chr20:g.63414924C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414924C>T , CM000682.2:g.63414924C>T	GRCh38
NC_000020.10:g.62046277C>T , CM000682.1:g.62046277C>T	GRCh37
NC_000020.9:g.61516721C>T	NCBI36
NG_009004.1:g.62717G>A
NG_009004.2:g.62717G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1450G>A	ENSP00000516702.1:p.Ala484Thr
ENST00000359125.7:c.1504G>A MANE Select	ENSP00000352035.2:p.Ala502Thr
ENST00000637193.1:c.901G>A	ENSP00000490734.1:p.Ala301Thr
ENST00000344462.8:c.1414G>A	ENSP00000339611.4:p.Ala472Thr
ENST00000357249.6:c.1072G>A	ENSP00000349789.3:p.Ala358Thr
ENST00000359125.6:c.1504G>A	ENSP00000352035.2:p.Ala502Thr
ENST00000360480.7:c.1420G>A	ENSP00000353668.3:p.Ala474Thr
ENST00000370224.5:c.1420G>A	ENSP00000359244.2:p.Ala474Thr
ENST00000625514.2:c.1384G>A	ENSP00000486040.1:p.Ala462Thr
ENST00000626839.2:c.1450G>A	ENSP00000486706.1:p.Ala484Thr
ENST00000627221.2:c.564G>A
ENST00000629241.2:c.1420G>A	ENSP00000487142.1:p.Ala474Thr
ENST00000629318.1:c.112G>A	ENSP00000487384.1:p.Ala38Thr
ENST00000629676.2:c.1420G>A	ENSP00000486194.1:p.Ala474Thr
NM_004518.4:c.1420G>A	NP_004509.2:p.Ala474Thr
NM_172106.1:c.1450G>A	NP_742104.1:p.Ala484Thr
NM_172107.2:c.1504G>A	NP_742105.1:p.Ala502Thr
NM_172108.3:c.1414G>A	NP_742106.1:p.Ala472Thr
XM_006723787.1:c.1504G>A	XP_006723850.1:p.Ala502Thr
XM_011528807.1:c.1504G>A	XP_011527109.1:p.Ala502Thr
XM_011528808.1:c.1504G>A	XP_011527110.1:p.Ala502Thr
XM_011528809.1:c.1474G>A	XP_011527111.1:p.Ala492Thr
XM_011528810.1:c.1450G>A	XP_011527112.1:p.Ala484Thr
XM_011528811.1:c.1420G>A	XP_011527113.1:p.Ala474Thr
XM_011528812.1:c.1504G>A	XP_011527114.1:p.Ala502Thr
XM_011528813.1:c.1378G>A	XP_011527115.1:p.Ala460Thr
XM_011528814.1:c.985G>A	XP_011527116.1:p.Ala329Thr
XM_011528815.1:c.1504G>A	XP_011527117.1:p.Ala502Thr
NM_004518.5:c.1420G>A	NP_004509.2:p.Ala474Thr
NM_172106.2:c.1450G>A	NP_742104.1:p.Ala484Thr
NM_172107.3:c.1504G>A	NP_742105.1:p.Ala502Thr
NM_172108.4:c.1414G>A	NP_742106.1:p.Ala472Thr
XM_011528810.2:c.1450G>A	XP_011527112.1:p.Ala484Thr
XM_011528811.2:c.1420G>A	XP_011527113.1:p.Ala474Thr
XM_017027841.2:c.1450G>A	XP_016883330.1:p.Ala484Thr
XM_017027842.2:c.1450G>A	XP_016883331.1:p.Ala484Thr
XM_017027843.1:c.1381G>A	XP_016883332.1:p.Ala461Thr
XM_017027844.2:c.1450G>A	XP_016883333.1:p.Ala484Thr
XM_017027845.1:c.412G>A	XP_016883334.1:p.Ala138Thr
NM_004518.6:c.1420G>A	NP_004509.2:p.Ala474Thr
NM_172106.3:c.1450G>A	NP_742104.1:p.Ala484Thr
NM_172107.4:c.1504G>A MANE Select	NP_742105.1:p.Ala502Thr
NM_172108.5:c.1414G>A	NP_742106.1:p.Ala472Thr
NM_001382235.1:c.1450G>A	NP_001369164.1:p.Ala484Thr