Canonical Allele Identifier: CA409639259

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038637C>G (hg19) ; chr20:g.63407284C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407284C>G , CM000682.2:g.63407284C>G	GRCh38
NC_000020.10:g.62038637C>G , CM000682.1:g.62038637C>G	GRCh37
NC_000020.9:g.61509081C>G	NCBI36
NG_009004.1:g.70357G>C
NG_009004.2:g.70357G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2033G>C	ENSP00000516702.1:p.Gly678Ala
ENST00000359125.7:c.1979G>C MANE Select	ENSP00000352035.2:p.Gly660Ala
ENST00000637193.1:c.1376G>C	ENSP00000490734.1:p.Gly459Ala
ENST00000344462.8:c.1886G>C	ENSP00000339611.4:p.Gly629Ala
ENST00000357249.6:c.1547G>C	ENSP00000349789.3:p.Gly516Ala
ENST00000359125.6:c.1979G>C	ENSP00000352035.2:p.Gly660Ala
ENST00000360480.7:c.1895G>C	ENSP00000353668.3:p.Gly632Ala
ENST00000370224.5:c.2003G>C	ENSP00000359244.2:p.Gly668Ala
ENST00000625514.2:c.1967G>C	ENSP00000486040.1:p.Gly656Ala
ENST00000626839.2:c.1925G>C	ENSP00000486706.1:p.Gly642Ala
ENST00000629241.2:c.1895G>C	ENSP00000487142.1:p.Gly632Ala
ENST00000629676.2:c.1679+6166G>C	ENSP00000486194.1:n.1679+6166G>C
NM_004518.4:c.1895G>C	NP_004509.2:p.Gly632Ala
NM_172106.1:c.1925G>C	NP_742104.1:p.Gly642Ala
NM_172107.2:c.1979G>C	NP_742105.1:p.Gly660Ala
NM_172108.3:c.1886G>C	NP_742106.1:p.Gly629Ala
XM_006723787.1:c.2021G>C	XP_006723850.1:p.Gly674Ala
XM_011528807.1:c.2087G>C	XP_011527109.1:p.Gly696Ala
XM_011528808.1:c.2084G>C	XP_011527110.1:p.Gly695Ala
XM_011528809.1:c.2057G>C	XP_011527111.1:p.Gly686Ala
XM_011528810.1:c.2033G>C	XP_011527112.1:p.Gly678Ala
XM_011528811.1:c.2003G>C	XP_011527113.1:p.Gly668Ala
XM_011528812.1:c.1976G>C	XP_011527114.1:p.Gly659Ala
XM_011528813.1:c.1961G>C	XP_011527115.1:p.Gly654Ala
XM_011528814.1:c.1568G>C	XP_011527116.1:p.Gly523Ala
NM_004518.5:c.1895G>C	NP_004509.2:p.Gly632Ala
NM_172106.2:c.1925G>C	NP_742104.1:p.Gly642Ala
NM_172107.3:c.1979G>C	NP_742105.1:p.Gly660Ala
NM_172108.4:c.1886G>C	NP_742106.1:p.Gly629Ala
XM_011528810.2:c.2033G>C	XP_011527112.1:p.Gly678Ala
XM_011528811.2:c.2003G>C	XP_011527113.1:p.Gly668Ala
XM_017027841.2:c.2030G>C	XP_016883330.1:p.Gly677Ala
XM_017027842.2:c.1967G>C	XP_016883331.1:p.Gly656Ala
XM_017027843.1:c.1964G>C	XP_016883332.1:p.Gly655Ala
XM_017027844.2:c.1922G>C	XP_016883333.1:p.Gly641Ala
XM_017027845.1:c.995G>C	XP_016883334.1:p.Gly332Ala
NM_004518.6:c.1895G>C	NP_004509.2:p.Gly632Ala
NM_172106.3:c.1925G>C	NP_742104.1:p.Gly642Ala
NM_172107.4:c.1979G>C MANE Select	NP_742105.1:p.Gly660Ala
NM_172108.5:c.1886G>C	NP_742106.1:p.Gly629Ala
NM_001382235.1:c.2033G>C	NP_001369164.1:p.Gly678Ala