Canonical Allele Identifier: CA409638828

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038466G>A (hg19) ; chr20:g.63407113G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407113G>A , CM000682.2:g.63407113G>A	GRCh38
NC_000020.10:g.62038466G>A , CM000682.1:g.62038466G>A	GRCh37
NC_000020.9:g.61508910G>A	NCBI36
NG_009004.1:g.70528C>T
NG_009004.2:g.70528C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2204C>T	ENSP00000516702.1:p.Ser735Phe
ENST00000359125.7:c.2150C>T MANE Select	ENSP00000352035.2:p.Ser717Phe
ENST00000637193.1:c.1547C>T	ENSP00000490734.1:p.Ser516Phe
ENST00000344462.8:c.2057C>T	ENSP00000339611.4:p.Ser686Phe
ENST00000357249.6:c.1718C>T	ENSP00000349789.3:p.Ser573Phe
ENST00000359125.6:c.2150C>T	ENSP00000352035.2:p.Ser717Phe
ENST00000360480.7:c.2066C>T	ENSP00000353668.3:p.Ser689Phe
ENST00000370224.5:c.2174C>T	ENSP00000359244.2:p.Ser725Phe
ENST00000625514.2:c.2138C>T	ENSP00000486040.1:p.Ser713Phe
ENST00000626839.2:c.2096C>T	ENSP00000486706.1:p.Ser699Phe
ENST00000629241.2:c.2066C>T	ENSP00000487142.1:p.Ser689Phe
ENST00000629676.2:c.1680-6270C>T	ENSP00000486194.1:n.1680-6270C>T
NM_004518.4:c.2066C>T	NP_004509.2:p.Ser689Phe
NM_172106.1:c.2096C>T	NP_742104.1:p.Ser699Phe
NM_172107.2:c.2150C>T	NP_742105.1:p.Ser717Phe
NM_172108.3:c.2057C>T	NP_742106.1:p.Ser686Phe
XM_006723787.1:c.2192C>T	XP_006723850.1:p.Ser731Phe
XM_011528807.1:c.2258C>T	XP_011527109.1:p.Ser753Phe
XM_011528808.1:c.2255C>T	XP_011527110.1:p.Ser752Phe
XM_011528809.1:c.2228C>T	XP_011527111.1:p.Ser743Phe
XM_011528810.1:c.2204C>T	XP_011527112.1:p.Ser735Phe
XM_011528811.1:c.2174C>T	XP_011527113.1:p.Ser725Phe
XM_011528812.1:c.2147C>T	XP_011527114.1:p.Ser716Phe
XM_011528813.1:c.2132C>T	XP_011527115.1:p.Ser711Phe
XM_011528814.1:c.1739C>T	XP_011527116.1:p.Ser580Phe
NM_004518.5:c.2066C>T	NP_004509.2:p.Ser689Phe
NM_172106.2:c.2096C>T	NP_742104.1:p.Ser699Phe
NM_172107.3:c.2150C>T	NP_742105.1:p.Ser717Phe
NM_172108.4:c.2057C>T	NP_742106.1:p.Ser686Phe
XM_011528810.2:c.2204C>T	XP_011527112.1:p.Ser735Phe
XM_011528811.2:c.2174C>T	XP_011527113.1:p.Ser725Phe
XM_017027841.2:c.2201C>T	XP_016883330.1:p.Ser734Phe
XM_017027842.2:c.2138C>T	XP_016883331.1:p.Ser713Phe
XM_017027843.1:c.2135C>T	XP_016883332.1:p.Ser712Phe
XM_017027844.2:c.2093C>T	XP_016883333.1:p.Ser698Phe
XM_017027845.1:c.1166C>T	XP_016883334.1:p.Ser389Phe
NM_004518.6:c.2066C>T	NP_004509.2:p.Ser689Phe
NM_172106.3:c.2096C>T	NP_742104.1:p.Ser699Phe
NM_172107.4:c.2150C>T MANE Select	NP_742105.1:p.Ser717Phe
NM_172108.5:c.2057C>T	NP_742106.1:p.Ser686Phe
NM_001382235.1:c.2204C>T	NP_001369164.1:p.Ser735Phe