Canonical Allele Identifier: CA409639020

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038529G>C (hg19) ; chr20:g.63407176G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407176G>C , CM000682.2:g.63407176G>C	GRCh38
NC_000020.10:g.62038529G>C , CM000682.1:g.62038529G>C	GRCh37
NC_000020.9:g.61508973G>C	NCBI36
NG_009004.1:g.70465C>G
NG_009004.2:g.70465C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2141C>G	ENSP00000516702.1:p.Thr714Arg
ENST00000359125.7:c.2087C>G MANE Select	ENSP00000352035.2:p.Thr696Arg
ENST00000637193.1:c.1484C>G	ENSP00000490734.1:p.Thr495Arg
ENST00000344462.8:c.1994C>G	ENSP00000339611.4:p.Thr665Arg
ENST00000357249.6:c.1655C>G	ENSP00000349789.3:p.Thr552Arg
ENST00000359125.6:c.2087C>G	ENSP00000352035.2:p.Thr696Arg
ENST00000360480.7:c.2003C>G	ENSP00000353668.3:p.Thr668Arg
ENST00000370224.5:c.2111C>G	ENSP00000359244.2:p.Thr704Arg
ENST00000625514.2:c.2075C>G	ENSP00000486040.1:p.Thr692Arg
ENST00000626839.2:c.2033C>G	ENSP00000486706.1:p.Thr678Arg
ENST00000629241.2:c.2003C>G	ENSP00000487142.1:p.Thr668Arg
ENST00000629676.2:c.1679+6274C>G	ENSP00000486194.1:n.1679+6274C>G
NM_004518.4:c.2003C>G	NP_004509.2:p.Thr668Arg
NM_172106.1:c.2033C>G	NP_742104.1:p.Thr678Arg
NM_172107.2:c.2087C>G	NP_742105.1:p.Thr696Arg
NM_172108.3:c.1994C>G	NP_742106.1:p.Thr665Arg
XM_006723787.1:c.2129C>G	XP_006723850.1:p.Thr710Arg
XM_011528807.1:c.2195C>G	XP_011527109.1:p.Thr732Arg
XM_011528808.1:c.2192C>G	XP_011527110.1:p.Thr731Arg
XM_011528809.1:c.2165C>G	XP_011527111.1:p.Thr722Arg
XM_011528810.1:c.2141C>G	XP_011527112.1:p.Thr714Arg
XM_011528811.1:c.2111C>G	XP_011527113.1:p.Thr704Arg
XM_011528812.1:c.2084C>G	XP_011527114.1:p.Thr695Arg
XM_011528813.1:c.2069C>G	XP_011527115.1:p.Thr690Arg
XM_011528814.1:c.1676C>G	XP_011527116.1:p.Thr559Arg
NM_004518.5:c.2003C>G	NP_004509.2:p.Thr668Arg
NM_172106.2:c.2033C>G	NP_742104.1:p.Thr678Arg
NM_172107.3:c.2087C>G	NP_742105.1:p.Thr696Arg
NM_172108.4:c.1994C>G	NP_742106.1:p.Thr665Arg
XM_011528810.2:c.2141C>G	XP_011527112.1:p.Thr714Arg
XM_011528811.2:c.2111C>G	XP_011527113.1:p.Thr704Arg
XM_017027841.2:c.2138C>G	XP_016883330.1:p.Thr713Arg
XM_017027842.2:c.2075C>G	XP_016883331.1:p.Thr692Arg
XM_017027843.1:c.2072C>G	XP_016883332.1:p.Thr691Arg
XM_017027844.2:c.2030C>G	XP_016883333.1:p.Thr677Arg
XM_017027845.1:c.1103C>G	XP_016883334.1:p.Thr368Arg
NM_004518.6:c.2003C>G	NP_004509.2:p.Thr668Arg
NM_172106.3:c.2033C>G	NP_742104.1:p.Thr678Arg
NM_172107.4:c.2087C>G MANE Select	NP_742105.1:p.Thr696Arg
NM_172108.5:c.1994C>G	NP_742106.1:p.Thr665Arg
NM_001382235.1:c.2141C>G	NP_001369164.1:p.Thr714Arg