Canonical Allele Identifier: CA409639427

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038685T>G (hg19) ; chr20:g.63407332T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407332T>G , CM000682.2:g.63407332T>G	GRCh38
NC_000020.10:g.62038685T>G , CM000682.1:g.62038685T>G	GRCh37
NC_000020.9:g.61509129T>G	NCBI36
NG_009004.1:g.70309A>C
NG_009004.2:g.70309A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706989.1:c.1985A>C	ENSP00000516702.1:p.Tyr662Ser
ENST00000359125.7:c.1931A>C MANE Select	ENSP00000352035.2:p.Tyr644Ser
ENST00000637193.1:c.1328A>C	ENSP00000490734.1:p.Tyr443Ser
ENST00000637338.1:n.88A>C
ENST00000344462.8:c.1838A>C	ENSP00000339611.4:p.Tyr613Ser
ENST00000357249.6:c.1499A>C	ENSP00000349789.3:p.Tyr500Ser
ENST00000359125.6:c.1931A>C	ENSP00000352035.2:p.Tyr644Ser
ENST00000360480.7:c.1847A>C	ENSP00000353668.3:p.Tyr616Ser
ENST00000370224.5:c.1955A>C	ENSP00000359244.2:p.Tyr652Ser
ENST00000625514.2:c.1919A>C	ENSP00000486040.1:p.Tyr640Ser
ENST00000626839.2:c.1877A>C	ENSP00000486706.1:p.Tyr626Ser
ENST00000629241.2:c.1847A>C	ENSP00000487142.1:p.Tyr616Ser
ENST00000629676.2:c.1679+6118A>C	ENSP00000486194.1:n.1679+6118A>C
NM_004518.4:c.1847A>C	NP_004509.2:p.Tyr616Ser
NM_172106.1:c.1877A>C	NP_742104.1:p.Tyr626Ser
NM_172107.2:c.1931A>C	NP_742105.1:p.Tyr644Ser
NM_172108.3:c.1838A>C	NP_742106.1:p.Tyr613Ser
XM_006723787.1:c.1973A>C	XP_006723850.1:p.Tyr658Ser
XM_011528807.1:c.2039A>C	XP_011527109.1:p.Tyr680Ser
XM_011528808.1:c.2036A>C	XP_011527110.1:p.Tyr679Ser
XM_011528809.1:c.2009A>C	XP_011527111.1:p.Tyr670Ser
XM_011528810.1:c.1985A>C	XP_011527112.1:p.Tyr662Ser
XM_011528811.1:c.1955A>C	XP_011527113.1:p.Tyr652Ser
XM_011528812.1:c.1928A>C	XP_011527114.1:p.Tyr643Ser
XM_011528813.1:c.1913A>C	XP_011527115.1:p.Tyr638Ser
XM_011528814.1:c.1520A>C	XP_011527116.1:p.Tyr507Ser
NM_004518.5:c.1847A>C	NP_004509.2:p.Tyr616Ser
NM_172106.2:c.1877A>C	NP_742104.1:p.Tyr626Ser
NM_172107.3:c.1931A>C	NP_742105.1:p.Tyr644Ser
NM_172108.4:c.1838A>C	NP_742106.1:p.Tyr613Ser
XM_011528810.2:c.1985A>C	XP_011527112.1:p.Tyr662Ser
XM_011528811.2:c.1955A>C	XP_011527113.1:p.Tyr652Ser
XM_017027841.2:c.1982A>C	XP_016883330.1:p.Tyr661Ser
XM_017027842.2:c.1919A>C	XP_016883331.1:p.Tyr640Ser
XM_017027843.1:c.1916A>C	XP_016883332.1:p.Tyr639Ser
XM_017027844.2:c.1874A>C	XP_016883333.1:p.Tyr625Ser
XM_017027845.1:c.947A>C	XP_016883334.1:p.Tyr316Ser
NM_004518.6:c.1847A>C	NP_004509.2:p.Tyr616Ser
NM_172106.3:c.1877A>C	NP_742104.1:p.Tyr626Ser
NM_172107.4:c.1931A>C MANE Select	NP_742105.1:p.Tyr644Ser
NM_172108.5:c.1838A>C	NP_742106.1:p.Tyr613Ser
NM_001382235.1:c.1985A>C	NP_001369164.1:p.Tyr662Ser