Canonical Allele Identifier: CA409636984

Gene: KCNQ2

Linked Data

• MyVariant Identifiers: chr20:g.62038157C>G (hg19) ; chr20:g.63406804C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63406804C>G , CM000682.2:g.63406804C>G	GRCh38
NC_000020.10:g.62038157C>G , CM000682.1:g.62038157C>G	GRCh37
NC_000020.9:g.61508601C>G	NCBI36
NG_009004.1:g.70837G>C
NG_009004.2:g.70837G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.2513G>C	ENSP00000516702.1:p.Cys838Ser
ENST00000359125.7:c.2459G>C MANE Select	ENSP00000352035.2:p.Cys820Ser
ENST00000637193.1:c.1856G>C	ENSP00000490734.1:p.Cys619Ser
ENST00000344462.8:c.2366G>C	ENSP00000339611.4:p.Cys789Ser
ENST00000357249.6:c.2027G>C	ENSP00000349789.3:p.Cys676Ser
ENST00000359125.6:c.2459G>C	ENSP00000352035.2:p.Cys820Ser
ENST00000360480.7:c.2375G>C	ENSP00000353668.3:p.Cys792Ser
ENST00000370224.5:c.2241+242G>C	ENSP00000359244.2:n.2241+242G>C
ENST00000625514.2:c.2205+242G>C	ENSP00000486040.1:n.2205+242G>C
ENST00000626839.2:c.2405G>C	ENSP00000486706.1:p.Cys802Ser
ENST00000629241.2:c.2133+242G>C	ENSP00000487142.1:n.2133+242G>C
ENST00000629676.2:c.1680-5961G>C	ENSP00000486194.1:n.1680-5961G>C
NM_004518.4:c.2375G>C	NP_004509.2:p.Cys792Ser
NM_172106.1:c.2405G>C	NP_742104.1:p.Cys802Ser
NM_172107.2:c.2459G>C	NP_742105.1:p.Cys820Ser
NM_172108.3:c.2366G>C	NP_742106.1:p.Cys789Ser
XM_006723787.1:c.2501G>C	XP_006723850.1:p.Cys834Ser
XM_011528807.1:c.2567G>C	XP_011527109.1:p.Cys856Ser
XM_011528808.1:c.2564G>C	XP_011527110.1:p.Cys855Ser
XM_011528809.1:c.2537G>C	XP_011527111.1:p.Cys846Ser
XM_011528810.1:c.2513G>C	XP_011527112.1:p.Cys838Ser
XM_011528811.1:c.2483G>C	XP_011527113.1:p.Cys828Ser
XM_011528812.1:c.2456G>C	XP_011527114.1:p.Cys819Ser
XM_011528813.1:c.2441G>C	XP_011527115.1:p.Cys814Ser
XM_011528814.1:c.2048G>C	XP_011527116.1:p.Cys683Ser
NM_004518.5:c.2375G>C	NP_004509.2:p.Cys792Ser
NM_172106.2:c.2405G>C	NP_742104.1:p.Cys802Ser
NM_172107.3:c.2459G>C	NP_742105.1:p.Cys820Ser
NM_172108.4:c.2366G>C	NP_742106.1:p.Cys789Ser
XM_011528810.2:c.2513G>C	XP_011527112.1:p.Cys838Ser
XM_011528811.2:c.2483G>C	XP_011527113.1:p.Cys828Ser
XM_017027841.2:c.2510G>C	XP_016883330.1:p.Cys837Ser
XM_017027842.2:c.2447G>C	XP_016883331.1:p.Cys816Ser
XM_017027843.1:c.2444G>C	XP_016883332.1:p.Cys815Ser
XM_017027844.2:c.2402G>C	XP_016883333.1:p.Cys801Ser
XM_017027845.1:c.1475G>C	XP_016883334.1:p.Cys492Ser
NM_004518.6:c.2375G>C	NP_004509.2:p.Cys792Ser
NM_172106.3:c.2405G>C	NP_742104.1:p.Cys802Ser
NM_172107.4:c.2459G>C MANE Select	NP_742105.1:p.Cys820Ser
NM_172108.5:c.2366G>C	NP_742106.1:p.Cys789Ser
NM_001382235.1:c.2513G>C	NP_001369164.1:p.Cys838Ser