Canonical Allele Identifier: CA1139666778

Gene: KCNQ2

Linked Data

• ClinVar Variation Id: 948360
• ClinVar RCV Id: RCV001219597
• dbSNP Id: rs2080213813

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63414191del , CM000682.2:g.63414191del	GRCh38
NC_000020.10:g.62045544del , CM000682.1:g.62045544del	GRCh37
NC_000020.9:g.61515988del	NCBI36
NG_009004.1:g.63450del
NG_009004.2:g.63450del

Transcript Alleles

HGVS	Amino-acid change
ENST00000706989.1:c.1474del	ENSP00000516702.1:p.Ala492GlnfsTer19
ENST00000359125.7:c.1528del MANE Select	ENSP00000352035.2:p.Ala510GlnfsTer19
ENST00000637193.1:c.925del	ENSP00000490734.1:p.Ala309GlnfsTer19
ENST00000344462.8:c.1436-1del	ENSP00000339611.4:n.1436-1del
ENST00000357249.6:c.1096del	ENSP00000349789.3:p.Ala366GlnfsTer19
ENST00000359125.6:c.1528del	ENSP00000352035.2:p.Ala510GlnfsTer19
ENST00000360480.7:c.1444del	ENSP00000353668.3:p.Ala482GlnfsTer19
ENST00000370224.5:c.1444del	ENSP00000359244.2:p.Ala482GlnfsTer19
ENST00000625514.2:c.1408del	ENSP00000486040.1:p.Ala470GlnfsTer19
ENST00000626839.2:c.1474del	ENSP00000486706.1:p.Ala492GlnfsTer19
ENST00000627221.2:c.586-1del
ENST00000629241.2:c.1444del	ENSP00000487142.1:p.Ala482GlnfsTer19
ENST00000629318.1:c.136del	ENSP00000487384.1:p.Ala46GlnfsTer19
ENST00000629676.2:c.1444del	ENSP00000486194.1:p.Ala482GlnfsTer19
NM_004518.4:c.1444del	NP_004509.2:p.Ala482GlnfsTer19
NM_172106.1:c.1474del	NP_742104.1:p.Ala492GlnfsTer19
NM_172107.2:c.1528del	NP_742105.1:p.Ala510GlnfsTer19
NM_172108.3:c.1436-1del	NP_742106.1:n.1436-1del
XM_006723787.1:c.1528del	XP_006723850.1:p.Ala510GlnfsTer19
XM_011528807.1:c.1528del	XP_011527109.1:p.Ala510GlnfsTer19
XM_011528808.1:c.1526-1del	XP_011527110.1:n.1526-1del
XM_011528809.1:c.1498del	XP_011527111.1:p.Ala500GlnfsTer19
XM_011528810.1:c.1474del	XP_011527112.1:p.Ala492GlnfsTer19
XM_011528811.1:c.1444del	XP_011527113.1:p.Ala482GlnfsTer19
XM_011528812.1:c.1526-1del	XP_011527114.1:n.1526-1del
XM_011528813.1:c.1402del	XP_011527115.1:p.Ala468GlnfsTer19
XM_011528814.1:c.1009del	XP_011527116.1:p.Ala337GlnfsTer19
XM_011528815.1:c.1528del	XP_011527117.1:p.Ala510GlnfsTer19
NM_004518.5:c.1444del	NP_004509.2:p.Ala482GlnfsTer19
NM_172106.2:c.1474del	NP_742104.1:p.Ala492GlnfsTer19
NM_172107.3:c.1528del	NP_742105.1:p.Ala510GlnfsTer19
NM_172108.4:c.1436-1del	NP_742106.1:n.1436-1del
XM_011528810.2:c.1474del	XP_011527112.1:p.Ala492GlnfsTer19
XM_011528811.2:c.1444del	XP_011527113.1:p.Ala482GlnfsTer19
XM_017027841.2:c.1472-1del	XP_016883330.1:n.1472-1del
XM_017027842.2:c.1474del	XP_016883331.1:p.Ala492GlnfsTer19
XM_017027843.1:c.1405del	XP_016883332.1:p.Ala469GlnfsTer19
XM_017027844.2:c.1472-1del	XP_016883333.1:n.1472-1del
XM_017027845.1:c.436del	XP_016883334.1:p.Ala146GlnfsTer19
NM_004518.6:c.1444del	NP_004509.2:p.Ala482GlnfsTer19
NM_172106.3:c.1474del	NP_742104.1:p.Ala492GlnfsTer19
NM_172107.4:c.1528del MANE Select	NP_742105.1:p.Ala510GlnfsTer19
NM_172108.5:c.1436-1del	NP_742106.1:n.1436-1del
NM_001382235.1:c.1474del	NP_001369164.1:p.Ala492GlnfsTer19