Canonical Allele Identifier: CA409639042

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038538C>G (hg19) ; chr20:g.63407185C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407185C>G , CM000682.2:g.63407185C>G	GRCh38
NC_000020.10:g.62038538C>G , CM000682.1:g.62038538C>G	GRCh37
NC_000020.9:g.61508982C>G	NCBI36
NG_009004.1:g.70456G>C
NG_009004.2:g.70456G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2132G>C	ENSP00000516702.1:p.Ser711Thr
ENST00000359125.7:c.2078G>C MANE Select	ENSP00000352035.2:p.Ser693Thr
ENST00000637193.1:c.1475G>C	ENSP00000490734.1:p.Ser492Thr
ENST00000344462.8:c.1985G>C	ENSP00000339611.4:p.Ser662Thr
ENST00000357249.6:c.1646G>C	ENSP00000349789.3:p.Ser549Thr
ENST00000359125.6:c.2078G>C	ENSP00000352035.2:p.Ser693Thr
ENST00000360480.7:c.1994G>C	ENSP00000353668.3:p.Ser665Thr
ENST00000370224.5:c.2102G>C	ENSP00000359244.2:p.Ser701Thr
ENST00000625514.2:c.2066G>C	ENSP00000486040.1:p.Ser689Thr
ENST00000626839.2:c.2024G>C	ENSP00000486706.1:p.Ser675Thr
ENST00000629241.2:c.1994G>C	ENSP00000487142.1:p.Ser665Thr
ENST00000629676.2:c.1679+6265G>C	ENSP00000486194.1:n.1679+6265G>C
NM_004518.4:c.1994G>C	NP_004509.2:p.Ser665Thr
NM_172106.1:c.2024G>C	NP_742104.1:p.Ser675Thr
NM_172107.2:c.2078G>C	NP_742105.1:p.Ser693Thr
NM_172108.3:c.1985G>C	NP_742106.1:p.Ser662Thr
XM_006723787.1:c.2120G>C	XP_006723850.1:p.Ser707Thr
XM_011528807.1:c.2186G>C	XP_011527109.1:p.Ser729Thr
XM_011528808.1:c.2183G>C	XP_011527110.1:p.Ser728Thr
XM_011528809.1:c.2156G>C	XP_011527111.1:p.Ser719Thr
XM_011528810.1:c.2132G>C	XP_011527112.1:p.Ser711Thr
XM_011528811.1:c.2102G>C	XP_011527113.1:p.Ser701Thr
XM_011528812.1:c.2075G>C	XP_011527114.1:p.Ser692Thr
XM_011528813.1:c.2060G>C	XP_011527115.1:p.Ser687Thr
XM_011528814.1:c.1667G>C	XP_011527116.1:p.Ser556Thr
NM_004518.5:c.1994G>C	NP_004509.2:p.Ser665Thr
NM_172106.2:c.2024G>C	NP_742104.1:p.Ser675Thr
NM_172107.3:c.2078G>C	NP_742105.1:p.Ser693Thr
NM_172108.4:c.1985G>C	NP_742106.1:p.Ser662Thr
XM_011528810.2:c.2132G>C	XP_011527112.1:p.Ser711Thr
XM_011528811.2:c.2102G>C	XP_011527113.1:p.Ser701Thr
XM_017027841.2:c.2129G>C	XP_016883330.1:p.Ser710Thr
XM_017027842.2:c.2066G>C	XP_016883331.1:p.Ser689Thr
XM_017027843.1:c.2063G>C	XP_016883332.1:p.Ser688Thr
XM_017027844.2:c.2021G>C	XP_016883333.1:p.Ser674Thr
XM_017027845.1:c.1094G>C	XP_016883334.1:p.Ser365Thr
NM_004518.6:c.1994G>C	NP_004509.2:p.Ser665Thr
NM_172106.3:c.2024G>C	NP_742104.1:p.Ser675Thr
NM_172107.4:c.2078G>C MANE Select	NP_742105.1:p.Ser693Thr
NM_172108.5:c.1985G>C	NP_742106.1:p.Ser662Thr
NM_001382235.1:c.2132G>C	NP_001369164.1:p.Ser711Thr