Canonical Allele Identifier: CA409638296

Gene: KCNQ2

Linked Data

• gnomAD v4: 20-63407024-C-A
• MyVariant Identifiers: chr20:g.62038377C>A (hg19) ; chr20:g.63407024C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407024C>A , CM000682.2:g.63407024C>A	GRCh38
NC_000020.10:g.62038377C>A , CM000682.1:g.62038377C>A	GRCh37
NC_000020.9:g.61508821C>A	NCBI36
NG_009004.1:g.70617G>T
NG_009004.2:g.70617G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2293G>T	ENSP00000516702.1:p.Ala765Ser
ENST00000359125.7:c.2239G>T MANE Select	ENSP00000352035.2:p.Ala747Ser
ENST00000637193.1:c.1636G>T	ENSP00000490734.1:p.Ala546Ser
ENST00000344462.8:c.2146G>T	ENSP00000339611.4:p.Ala716Ser
ENST00000357249.6:c.1807G>T	ENSP00000349789.3:p.Ala603Ser
ENST00000359125.6:c.2239G>T	ENSP00000352035.2:p.Ala747Ser
ENST00000360480.7:c.2155G>T	ENSP00000353668.3:p.Ala719Ser
ENST00000370224.5:c.2241+22G>T	ENSP00000359244.2:n.2241+22G>T
ENST00000625514.2:c.2205+22G>T	ENSP00000486040.1:n.2205+22G>T
ENST00000626839.2:c.2185G>T	ENSP00000486706.1:p.Ala729Ser
ENST00000629241.2:c.2133+22G>T	ENSP00000487142.1:n.2133+22G>T
ENST00000629676.2:c.1680-6181G>T	ENSP00000486194.1:n.1680-6181G>T
NM_004518.4:c.2155G>T	NP_004509.2:p.Ala719Ser
NM_172106.1:c.2185G>T	NP_742104.1:p.Ala729Ser
NM_172107.2:c.2239G>T	NP_742105.1:p.Ala747Ser
NM_172108.3:c.2146G>T	NP_742106.1:p.Ala716Ser
XM_006723787.1:c.2281G>T	XP_006723850.1:p.Ala761Ser
XM_011528807.1:c.2347G>T	XP_011527109.1:p.Ala783Ser
XM_011528808.1:c.2344G>T	XP_011527110.1:p.Ala782Ser
XM_011528809.1:c.2317G>T	XP_011527111.1:p.Ala773Ser
XM_011528810.1:c.2293G>T	XP_011527112.1:p.Ala765Ser
XM_011528811.1:c.2263G>T	XP_011527113.1:p.Ala755Ser
XM_011528812.1:c.2236G>T	XP_011527114.1:p.Ala746Ser
XM_011528813.1:c.2221G>T	XP_011527115.1:p.Ala741Ser
XM_011528814.1:c.1828G>T	XP_011527116.1:p.Ala610Ser
NM_004518.5:c.2155G>T	NP_004509.2:p.Ala719Ser
NM_172106.2:c.2185G>T	NP_742104.1:p.Ala729Ser
NM_172107.3:c.2239G>T	NP_742105.1:p.Ala747Ser
NM_172108.4:c.2146G>T	NP_742106.1:p.Ala716Ser
XM_011528810.2:c.2293G>T	XP_011527112.1:p.Ala765Ser
XM_011528811.2:c.2263G>T	XP_011527113.1:p.Ala755Ser
XM_017027841.2:c.2290G>T	XP_016883330.1:p.Ala764Ser
XM_017027842.2:c.2227G>T	XP_016883331.1:p.Ala743Ser
XM_017027843.1:c.2224G>T	XP_016883332.1:p.Ala742Ser
XM_017027844.2:c.2182G>T	XP_016883333.1:p.Ala728Ser
XM_017027845.1:c.1255G>T	XP_016883334.1:p.Ala419Ser
NM_004518.6:c.2155G>T	NP_004509.2:p.Ala719Ser
NM_172106.3:c.2185G>T	NP_742104.1:p.Ala729Ser
NM_172107.4:c.2239G>T MANE Select	NP_742105.1:p.Ala747Ser
NM_172108.5:c.2146G>T	NP_742106.1:p.Ala716Ser
NM_001382235.1:c.2293G>T	NP_001369164.1:p.Ala765Ser