Canonical Allele Identifier: CA409646687

Gene: KCNQ2

Linked Data

• dbSNP Id: rs2145556609
• MyVariant Identifiers: chr20:g.62046391T>C (hg19) ; chr20:g.63415038T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63415038T>C , CM000682.2:g.63415038T>C	GRCh38
NC_000020.10:g.62046391T>C , CM000682.1:g.62046391T>C	GRCh37
NC_000020.9:g.61516835T>C	NCBI36
NG_009004.1:g.62603A>G
NG_009004.2:g.62603A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1336A>G	ENSP00000516702.1:p.Arg446Gly
ENST00000359125.7:c.1390A>G MANE Select	ENSP00000352035.2:p.Arg464Gly
ENST00000637193.1:c.787A>G	ENSP00000490734.1:p.Arg263Gly
ENST00000344462.8:c.1300A>G	ENSP00000339611.4:p.Arg434Gly
ENST00000357249.6:c.958A>G	ENSP00000349789.3:p.Arg320Gly
ENST00000359125.6:c.1390A>G	ENSP00000352035.2:p.Arg464Gly
ENST00000360480.7:c.1306A>G	ENSP00000353668.3:p.Arg436Gly
ENST00000370224.5:c.1306A>G	ENSP00000359244.2:p.Arg436Gly
ENST00000625514.2:c.1270A>G	ENSP00000486040.1:p.Arg424Gly
ENST00000626839.2:c.1336A>G	ENSP00000486706.1:p.Arg446Gly
ENST00000627221.2:c.450A>G
ENST00000629241.2:c.1306A>G	ENSP00000487142.1:p.Arg436Gly
ENST00000629676.2:c.1306A>G	ENSP00000486194.1:p.Arg436Gly
NM_004518.4:c.1306A>G	NP_004509.2:p.Arg436Gly
NM_172106.1:c.1336A>G	NP_742104.1:p.Arg446Gly
NM_172107.2:c.1390A>G	NP_742105.1:p.Arg464Gly
NM_172108.3:c.1300A>G	NP_742106.1:p.Arg434Gly
XM_006723787.1:c.1390A>G	XP_006723850.1:p.Arg464Gly
XM_011528807.1:c.1390A>G	XP_011527109.1:p.Arg464Gly
XM_011528808.1:c.1390A>G	XP_011527110.1:p.Arg464Gly
XM_011528809.1:c.1360A>G	XP_011527111.1:p.Arg454Gly
XM_011528810.1:c.1336A>G	XP_011527112.1:p.Arg446Gly
XM_011528811.1:c.1306A>G	XP_011527113.1:p.Arg436Gly
XM_011528812.1:c.1390A>G	XP_011527114.1:p.Arg464Gly
XM_011528813.1:c.1264A>G	XP_011527115.1:p.Arg422Gly
XM_011528814.1:c.871A>G	XP_011527116.1:p.Arg291Gly
XM_011528815.1:c.1390A>G	XP_011527117.1:p.Arg464Gly
NM_004518.5:c.1306A>G	NP_004509.2:p.Arg436Gly
NM_172106.2:c.1336A>G	NP_742104.1:p.Arg446Gly
NM_172107.3:c.1390A>G	NP_742105.1:p.Arg464Gly
NM_172108.4:c.1300A>G	NP_742106.1:p.Arg434Gly
XM_011528810.2:c.1336A>G	XP_011527112.1:p.Arg446Gly
XM_011528811.2:c.1306A>G	XP_011527113.1:p.Arg436Gly
XM_017027841.2:c.1336A>G	XP_016883330.1:p.Arg446Gly
XM_017027842.2:c.1336A>G	XP_016883331.1:p.Arg446Gly
XM_017027843.1:c.1267A>G	XP_016883332.1:p.Arg423Gly
XM_017027844.2:c.1336A>G	XP_016883333.1:p.Arg446Gly
XM_017027845.1:c.298A>G	XP_016883334.1:p.Arg100Gly
NM_004518.6:c.1306A>G	NP_004509.2:p.Arg436Gly
NM_172106.3:c.1336A>G	NP_742104.1:p.Arg446Gly
NM_172107.4:c.1390A>G MANE Select	NP_742105.1:p.Arg464Gly
NM_172108.5:c.1300A>G	NP_742106.1:p.Arg434Gly
NM_001382235.1:c.1336A>G	NP_001369164.1:p.Arg446Gly