Canonical Allele Identifier: CA511339743

Gene: KCNQ2

Linked Data

• dbSNP Id: rs756622558
• gnomAD v2: 20-62046388-G-T
• gnomAD v4: 20-63415035-G-T
• MyVariant Identifiers: chr20:g.62046388G>T (hg19) ; chr20:g.63415035G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63415035G>T , CM000682.2:g.63415035G>T	GRCh38
NC_000020.10:g.62046388G>T , CM000682.1:g.62046388G>T	GRCh37
NC_000020.9:g.61516832G>T	NCBI36
NG_009004.1:g.62606C>A
NG_009004.2:g.62606C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1339C>A	ENSP00000516702.1:p.Arg447=
ENST00000359125.7:c.1393C>A MANE Select	ENSP00000352035.2:p.Arg465=
ENST00000637193.1:c.790C>A	ENSP00000490734.1:p.Arg264=
ENST00000344462.8:c.1303C>A	ENSP00000339611.4:p.Arg435=
ENST00000357249.6:c.961C>A	ENSP00000349789.3:p.Arg321=
ENST00000359125.6:c.1393C>A	ENSP00000352035.2:p.Arg465=
ENST00000360480.7:c.1309C>A	ENSP00000353668.3:p.Arg437=
ENST00000370224.5:c.1309C>A	ENSP00000359244.2:p.Arg437=
ENST00000625514.2:c.1273C>A	ENSP00000486040.1:p.Arg425=
ENST00000626839.2:c.1339C>A	ENSP00000486706.1:p.Arg447=
ENST00000627221.2:c.453C>A
ENST00000629241.2:c.1309C>A	ENSP00000487142.1:p.Arg437=
ENST00000629318.1:c.1C>A	ENSP00000487384.1:p.Arg1=
ENST00000629676.2:c.1309C>A	ENSP00000486194.1:p.Arg437=
NM_004518.4:c.1309C>A	NP_004509.2:p.Arg437=
NM_172106.1:c.1339C>A	NP_742104.1:p.Arg447=
NM_172107.2:c.1393C>A	NP_742105.1:p.Arg465=
NM_172108.3:c.1303C>A	NP_742106.1:p.Arg435=
XM_006723787.1:c.1393C>A	XP_006723850.1:p.Arg465=
XM_011528807.1:c.1393C>A	XP_011527109.1:p.Arg465=
XM_011528808.1:c.1393C>A	XP_011527110.1:p.Arg465=
XM_011528809.1:c.1363C>A	XP_011527111.1:p.Arg455=
XM_011528810.1:c.1339C>A	XP_011527112.1:p.Arg447=
XM_011528811.1:c.1309C>A	XP_011527113.1:p.Arg437=
XM_011528812.1:c.1393C>A	XP_011527114.1:p.Arg465=
XM_011528813.1:c.1267C>A	XP_011527115.1:p.Arg423=
XM_011528814.1:c.874C>A	XP_011527116.1:p.Arg292=
XM_011528815.1:c.1393C>A	XP_011527117.1:p.Arg465=
NM_004518.5:c.1309C>A	NP_004509.2:p.Arg437=
NM_172106.2:c.1339C>A	NP_742104.1:p.Arg447=
NM_172107.3:c.1393C>A	NP_742105.1:p.Arg465=
NM_172108.4:c.1303C>A	NP_742106.1:p.Arg435=
XM_011528810.2:c.1339C>A	XP_011527112.1:p.Arg447=
XM_011528811.2:c.1309C>A	XP_011527113.1:p.Arg437=
XM_017027841.2:c.1339C>A	XP_016883330.1:p.Arg447=
XM_017027842.2:c.1339C>A	XP_016883331.1:p.Arg447=
XM_017027843.1:c.1270C>A	XP_016883332.1:p.Arg424=
XM_017027844.2:c.1339C>A	XP_016883333.1:p.Arg447=
XM_017027845.1:c.301C>A	XP_016883334.1:p.Arg101=
NM_004518.6:c.1309C>A	NP_004509.2:p.Arg437=
NM_172106.3:c.1339C>A	NP_742104.1:p.Arg447=
NM_172107.4:c.1393C>A MANE Select	NP_742105.1:p.Arg465=
NM_172108.5:c.1303C>A	NP_742106.1:p.Arg435=
NM_001382235.1:c.1339C>A	NP_001369164.1:p.Arg447=