Canonical Allele Identifier: CA409646530

Gene: KCNQ2

Linked Data

• dbSNP Id: rs2080240279
• MyVariant Identifiers: chr20:g.62046344C>G (hg19) ; chr20:g.63414991C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414991C>G , CM000682.2:g.63414991C>G	GRCh38
NC_000020.10:g.62046344C>G , CM000682.1:g.62046344C>G	GRCh37
NC_000020.9:g.61516788C>G	NCBI36
NG_009004.1:g.62650G>C
NG_009004.2:g.62650G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000706989.1:c.1383G>C	ENSP00000516702.1:p.Lys461Asn
ENST00000359125.7:c.1437G>C MANE Select	ENSP00000352035.2:p.Lys479Asn
ENST00000637193.1:c.834G>C	ENSP00000490734.1:p.Lys278Asn
ENST00000344462.8:c.1347G>C	ENSP00000339611.4:p.Lys449Asn
ENST00000357249.6:c.1005G>C	ENSP00000349789.3:p.Lys335Asn
ENST00000359125.6:c.1437G>C	ENSP00000352035.2:p.Lys479Asn
ENST00000360480.7:c.1353G>C	ENSP00000353668.3:p.Lys451Asn
ENST00000370224.5:c.1353G>C	ENSP00000359244.2:p.Lys451Asn
ENST00000625514.2:c.1317G>C	ENSP00000486040.1:p.Lys439Asn
ENST00000626839.2:c.1383G>C	ENSP00000486706.1:p.Lys461Asn
ENST00000627221.2:c.497G>C
ENST00000629241.2:c.1353G>C	ENSP00000487142.1:p.Lys451Asn
ENST00000629318.1:c.45G>C	ENSP00000487384.1:p.Lys15Asn
ENST00000629676.2:c.1353G>C	ENSP00000486194.1:p.Lys451Asn
NM_004518.4:c.1353G>C	NP_004509.2:p.Lys451Asn
NM_172106.1:c.1383G>C	NP_742104.1:p.Lys461Asn
NM_172107.2:c.1437G>C	NP_742105.1:p.Lys479Asn
NM_172108.3:c.1347G>C	NP_742106.1:p.Lys449Asn
XM_006723787.1:c.1437G>C	XP_006723850.1:p.Lys479Asn
XM_011528807.1:c.1437G>C	XP_011527109.1:p.Lys479Asn
XM_011528808.1:c.1437G>C	XP_011527110.1:p.Lys479Asn
XM_011528809.1:c.1407G>C	XP_011527111.1:p.Lys469Asn
XM_011528810.1:c.1383G>C	XP_011527112.1:p.Lys461Asn
XM_011528811.1:c.1353G>C	XP_011527113.1:p.Lys451Asn
XM_011528812.1:c.1437G>C	XP_011527114.1:p.Lys479Asn
XM_011528813.1:c.1311G>C	XP_011527115.1:p.Lys437Asn
XM_011528814.1:c.918G>C	XP_011527116.1:p.Lys306Asn
XM_011528815.1:c.1437G>C	XP_011527117.1:p.Lys479Asn
NM_004518.5:c.1353G>C	NP_004509.2:p.Lys451Asn
NM_172106.2:c.1383G>C	NP_742104.1:p.Lys461Asn
NM_172107.3:c.1437G>C	NP_742105.1:p.Lys479Asn
NM_172108.4:c.1347G>C	NP_742106.1:p.Lys449Asn
XM_011528810.2:c.1383G>C	XP_011527112.1:p.Lys461Asn
XM_011528811.2:c.1353G>C	XP_011527113.1:p.Lys451Asn
XM_017027841.2:c.1383G>C	XP_016883330.1:p.Lys461Asn
XM_017027842.2:c.1383G>C	XP_016883331.1:p.Lys461Asn
XM_017027843.1:c.1314G>C	XP_016883332.1:p.Lys438Asn
XM_017027844.2:c.1383G>C	XP_016883333.1:p.Lys461Asn
XM_017027845.1:c.345G>C	XP_016883334.1:p.Lys115Asn
NM_004518.6:c.1353G>C	NP_004509.2:p.Lys451Asn
NM_172106.3:c.1383G>C	NP_742104.1:p.Lys461Asn
NM_172107.4:c.1437G>C MANE Select	NP_742105.1:p.Lys479Asn
NM_172108.5:c.1347G>C	NP_742106.1:p.Lys449Asn
NM_001382235.1:c.1383G>C	NP_001369164.1:p.Lys461Asn