Canonical Allele Identifier: CA636343265

Gene: KCNQ2

Linked Data

• dbSNP Id: rs1568911158
• gnomAD v2: 20-62062759-CG-C
• gnomAD v4: 20-63431406-CG-C
• MyVariant Identifiers: chr20:g.62062760del (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.63431408del , CM000682.2:g.63431408del	GRCh38
NC_000020.10:g.62062761del , CM000682.1:g.62062761del	GRCh37
NC_000020.9:g.61533205del	NCBI36
NG_009004.1:g.46234del
NG_009004.2:g.46234del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000706989.1:c.1119-38del	ENSP00000516702.1:n.1119-38del
ENST00000359125.7:c.1119-38del MANE Select	ENSP00000352035.2:n.1119-38del
ENST00000636638.1:n.31+2039del
ENST00000637193.1:c.599+2402del	ENSP00000490734.1:n.599+2402del
ENST00000344462.8:c.1119-38del	ENSP00000339611.4:n.1119-38del
ENST00000357249.6:c.777-38del	ENSP00000349789.3:n.777-38del
ENST00000359125.6:c.1119-38del	ENSP00000352035.2:n.1119-38del
ENST00000360480.7:c.1118+2402del	ENSP00000353668.3:n.1118+2402del
ENST00000370221.3:n.1245-38del
ENST00000370224.5:c.1118+2402del	ENSP00000359244.2:n.1118+2402del
ENST00000625514.2:c.1118+2402del	ENSP00000486040.1:n.1118+2402del
ENST00000626839.2:c.1119-38del	ENSP00000486706.1:n.1119-38del
ENST00000627221.2:c.262+2402del
ENST00000629241.2:c.1118+2402del	ENSP00000487142.1:n.1118+2402del
ENST00000629676.2:c.1118+2402del	ENSP00000486194.1:n.1118+2402del
NM_004518.4:c.1118+2402del	NP_004509.2:n.1118+2402del
NM_172106.1:c.1119-38del	NP_742104.1:n.1119-38del
NM_172107.2:c.1119-38del	NP_742105.1:n.1119-38del
NM_172108.3:c.1119-38del	NP_742106.1:n.1119-38del
XM_006723787.1:c.1119-38del	XP_006723850.1:n.1119-38del
XM_011528807.1:c.1119-38del	XP_011527109.1:n.1119-38del
XM_011528808.1:c.1119-38del	XP_011527110.1:n.1119-38del
XM_011528809.1:c.1118+2402del	XP_011527111.1:n.1118+2402del
XM_011528810.1:c.1119-38del	XP_011527112.1:n.1119-38del
XM_011528811.1:c.1118+2402del	XP_011527113.1:n.1118+2402del
XM_011528812.1:c.1119-38del	XP_011527114.1:n.1119-38del
XM_011528813.1:c.993-38del	XP_011527115.1:n.993-38del
XM_011528814.1:c.600-38del	XP_011527116.1:n.600-38del
XM_011528815.1:c.1119-38del	XP_011527117.1:n.1119-38del
NM_004518.5:c.1118+2402del	NP_004509.2:n.1118+2402del
NM_172106.2:c.1119-38del	NP_742104.1:n.1119-38del
NM_172107.3:c.1119-38del	NP_742105.1:n.1119-38del
NM_172108.4:c.1119-38del	NP_742106.1:n.1119-38del
XM_011528810.2:c.1119-38del	XP_011527112.1:n.1119-38del
XM_011528811.2:c.1118+2402del	XP_011527113.1:n.1118+2402del
XM_017027841.2:c.1119-38del	XP_016883330.1:n.1119-38del
XM_017027842.2:c.1119-38del	XP_016883331.1:n.1119-38del
XM_017027843.1:c.1050-38del	XP_016883332.1:n.1050-38del
XM_017027844.2:c.1119-38del	XP_016883333.1:n.1119-38del
NM_004518.6:c.1118+2402del	NP_004509.2:n.1118+2402del
NM_172106.3:c.1119-38del	NP_742104.1:n.1119-38del
NM_172107.4:c.1119-38del MANE Select	NP_742105.1:n.1119-38del
NM_172108.5:c.1119-38del	NP_742106.1:n.1119-38del
NM_001382235.1:c.1119-38del	NP_001369164.1:n.1119-38del