Canonical Allele Identifier: CA409639227

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038623C>G (hg19) ; chr20:g.63407270C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63407270C>G , CM000682.2:g.63407270C>G	GRCh38
NC_000020.10:g.62038623C>G , CM000682.1:g.62038623C>G	GRCh37
NC_000020.9:g.61509067C>G	NCBI36
NG_009004.1:g.70371G>C
NG_009004.2:g.70371G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2047G>C	ENSP00000516702.1:p.Glu683Gln
ENST00000359125.7:c.1993G>C MANE Select	ENSP00000352035.2:p.Glu665Gln
ENST00000637193.1:c.1390G>C	ENSP00000490734.1:p.Glu464Gln
ENST00000344462.8:c.1900G>C	ENSP00000339611.4:p.Glu634Gln
ENST00000357249.6:c.1561G>C	ENSP00000349789.3:p.Glu521Gln
ENST00000359125.6:c.1993G>C	ENSP00000352035.2:p.Glu665Gln
ENST00000360480.7:c.1909G>C	ENSP00000353668.3:p.Glu637Gln
ENST00000370224.5:c.2017G>C	ENSP00000359244.2:p.Glu673Gln
ENST00000625514.2:c.1981G>C	ENSP00000486040.1:p.Glu661Gln
ENST00000626839.2:c.1939G>C	ENSP00000486706.1:p.Glu647Gln
ENST00000629241.2:c.1909G>C	ENSP00000487142.1:p.Glu637Gln
ENST00000629676.2:c.1679+6180G>C	ENSP00000486194.1:n.1679+6180G>C
NM_004518.4:c.1909G>C	NP_004509.2:p.Glu637Gln
NM_172106.1:c.1939G>C	NP_742104.1:p.Glu647Gln
NM_172107.2:c.1993G>C	NP_742105.1:p.Glu665Gln
NM_172108.3:c.1900G>C	NP_742106.1:p.Glu634Gln
XM_006723787.1:c.2035G>C	XP_006723850.1:p.Glu679Gln
XM_011528807.1:c.2101G>C	XP_011527109.1:p.Glu701Gln
XM_011528808.1:c.2098G>C	XP_011527110.1:p.Glu700Gln
XM_011528809.1:c.2071G>C	XP_011527111.1:p.Glu691Gln
XM_011528810.1:c.2047G>C	XP_011527112.1:p.Glu683Gln
XM_011528811.1:c.2017G>C	XP_011527113.1:p.Glu673Gln
XM_011528812.1:c.1990G>C	XP_011527114.1:p.Glu664Gln
XM_011528813.1:c.1975G>C	XP_011527115.1:p.Glu659Gln
XM_011528814.1:c.1582G>C	XP_011527116.1:p.Glu528Gln
NM_004518.5:c.1909G>C	NP_004509.2:p.Glu637Gln
NM_172106.2:c.1939G>C	NP_742104.1:p.Glu647Gln
NM_172107.3:c.1993G>C	NP_742105.1:p.Glu665Gln
NM_172108.4:c.1900G>C	NP_742106.1:p.Glu634Gln
XM_011528810.2:c.2047G>C	XP_011527112.1:p.Glu683Gln
XM_011528811.2:c.2017G>C	XP_011527113.1:p.Glu673Gln
XM_017027841.2:c.2044G>C	XP_016883330.1:p.Glu682Gln
XM_017027842.2:c.1981G>C	XP_016883331.1:p.Glu661Gln
XM_017027843.1:c.1978G>C	XP_016883332.1:p.Glu660Gln
XM_017027844.2:c.1936G>C	XP_016883333.1:p.Glu646Gln
XM_017027845.1:c.1009G>C	XP_016883334.1:p.Glu337Gln
NM_004518.6:c.1909G>C	NP_004509.2:p.Glu637Gln
NM_172106.3:c.1939G>C	NP_742104.1:p.Glu647Gln
NM_172107.4:c.1993G>C MANE Select	NP_742105.1:p.Glu665Gln
NM_172108.5:c.1900G>C	NP_742106.1:p.Glu634Gln
NM_001382235.1:c.2047G>C	NP_001369164.1:p.Glu683Gln